Genetic Variants Underlying Human Cognition and Methods of Use Thereof as Diagnostic and Therapeutic Targets

ABSTRACT

Compositions and methods for the detection and treatment of neurological disorders, including ASD, are provided.

This application claims priority under 35 U.S.C. §119(e) to U.S. Provisional Application 61/114,921, filed Nov. 14, 2008, the entire contents being incorporated herein by reference as though set forth in full.

Pursuant to 35 U.S.C. §202(c) it is acknowledged that the U.S. Government has certain rights in the invention described herein, which was made in part with funds from the National Institutes of Health, Grant Number P50HD055784-01.

FIELD OF THE INVENTION

This invention relates to the fields of genetics and the diagnosis and treatment of cognitive and neurological disorders. More specifically, the invention provides nucleic acids comprising copy number variations (CNVs) which are associated with the multiple disorders of human cognition and behavior and methods of use thereof in diagnostic and therapeutic applications.

BACKGROUND OF THE INVENTION

Several publications and patent documents are cited throughout the specification in order to describe the state of the art to which this invention pertains. Each of these citations is incorporated herein by reference as though set forth in full.

Neurologic diseases can result from disorders of the brain, spinal cord and nerves. Patients experiencing neurological disease may have trouble moving, speaking, swallowing, breathing or learning. Problems with memory, senses behavior or mood are also associated with neurological disorders. There are many different underlying causes of neurological dysfunction. These can include genetic mutation, exposure to toxic substances and injury.

There are more than 600 neurologic diseases. Major types include diseases caused by faulty genes, such as Huntington's disease and muscular dystrophy; aberrant embryonal development of the nervous system, such as spina bifida; degenerative diseases, where nerve cells are damaged or die, such as Parkinson's disease and Alzheimer's disease; diseases of the blood vessels that supply the brain, such as stroke; injuries to the spinal cord and brain; seizure disorders, such as epilepsy; cancer, such as brain tumors and infections, such as meningitis.

Multiple disorders of human cognition and behavior appear to be modulated by genetic factors. However, the manner by which genetic variation impacts disease is complex and poorly understood. Similarly elusive are the identity of specific genes that may be useful with regards to diagnosis and therapeutic intervention. It is an object of the invention to provide these genetic markers and to further characterize the alterations therein that lead to a loss of cognitive function and neurological development.

SUMMARY OF THE INVENTION

In accordance with the present invention, a method for detecting a propensity for developing a neurological disorder in a patient in need thereof is provided. An exemplary method entails detecting the presence of at least one CNV containing nucleic acid in a target polynucleotide wherein if said CNV is present, said patient has an increased risk for developing autism/ASD, wherein said CNV containing nucleic acid is selected from the group of CNVs that are either exclusive to or significantly overrepresented in neurological disorders, particularly autism spectrum disorder. (see Tables 1, 3, and 7).

In another embodiment of the invention, a method for identifying agents which alter neuronal signaling and/or morphology is provided. Such a method comprises providing cells expressing at least one of the CNVs listed above (step a); providing cells which express the cognate wild type sequences corresponding to the CNV (step b); contacting the cells from each sample with a test agent and analyzing whether said agent alters neuronal signaling and/or morphology of cells of step a) relative to those of step b), thereby identifying agents which alter neuronal signaling and morphology. Methods of treating patients having a neurological disorder via administration of pharmaceutical compositions comprising agents identified using the methods described herein in patients in need thereof are also encompassed by the present invention.

The invention also provides at least one isolated neurological disorder related CNV-containing nucleic acid selected from the group that are either exclusive to or significantly overrepresented in neurological disorders, particularly ASD (see Table 1 and Table 7). Such CNV containing nucleic acids may optionally be contained in a suitable expression vector for expression in neuronal cells. Alternatively, they may be immobilized on a solid support.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1—TaqMan experiments validate copy number calls determined by PennCNV. To validate results using an independent method we designed TaqMan assays to evaluate gene dosage. Results from representative experiments highlight results at loci at 1q21, 8q21, and 10q24. AGRE individual harboring deletions (red arrows) or gains (green arrows) are indicated.

FIG. 2—Rare exonic deletions (eDels) in NRXN1 and novel candidate genes alter predicted protein structures. For each of NRXN1 (a), CLCKNKA (b), GRIK5 (c), and GMPS (d) reference loci and encoded proteins (top) are contrasted against mutant loci and proteins (bottom; grey shading). Unique genomic deletions and corresponding protein truncations are highlighted in red and with black hatching, respectively. Schematized protein domains genes are as follows: NRXN1—Laminin G (orange hexagon), EGF-like (blue oval), 4.1 binding motif (green rectangle); CLCNKA—Chloride channel, core (orange rectangle), Cystathionine beta-synthase, core (blue pentagon); GRIK5—Extracellular ligand-binding receptor (orange oval), Ionotropic glutamate receptor (blue hexagon); GMPS—Glutamine amidotransferase class-I, C-terminal (orange rectangle), Exoenzyme S synthesis protein B/queuosine synthesis (blue rectangle), (GMP synthase, C-terminal (green rectangle). Rare exonic deletions (eDels) in NRXN1 and novel candidate genes alter predicted protein structures. For each of BZRAP1 and MDGA2 (c) reference loci and encoded proteins (top) are contrasted against mutant loci and corresponding proteins (bottom; grey shading). Unique genomic deletions and corresponding protein truncations are highlighted in red and with black hatching, respectively. Schematized protein domains genes are as follows: BZRAP1—Src homology-3 (orange square), Fibronectin, type III (blue oval); MDGA2—IG-like domains (blue pentagon), MAM aka Meprin/A5-protein/PTPmu (blue oval).

FIG. 3—Multi-dimensional scaling plot of AGRE affected subjects, with red cross highlighting subjects carrying the eDels. Subjects of European ancestry are clustered toward the right side of the triangle.

FIG. 4A—Observed replication unlikely to be attributable to chance alone. We performed 10,000 phenotype permutation trials on replication data and determined for each the number of loci harboring CNVs in cases but not controls. Thus, within each trial, the number of loci absent from controls in the replication cohort was determined. None of the permutation trials generated as many case-specific loci as observed in our actual dataset (n=14; p<0.0001). FIG. 4B. We also performed 10,000 phenotype permutation trials on replication data and determined for each the number of loci harboring CNVs exclusively in controls. During each trial a new set of control-specific loci was identified and the number of these absent from cases determined. We observed results comparable to those obtained experimentally (n=18) in 246 of 10,000 trials (p=0.02)

FIG. 5—Exonic deletions, although enriched in cases versus controls, show imperfect segregation with disease in multiplex families. Pedigrees for representative AGRE families harboring exonic deletions in BZRAP1 (A,B), kb), NRXN1 (C,D), and MDGA2 (E,F) are illustrated. Red filled circles correspond to exonic deletions. Black stars (upper right) highlight individuals for which CNV calls were not obtained (not genotyped or failing to meet criteria for quality control).

DETAILED DESCRIPTION OF THE INVENTION

The genetics underlying the neurological disorders (e.g., autism, autism spectrum disorder (ASD) schizophrenia, bipolar disorder, Tourette's syndrome, obsessive compulsive disorder (OCD) is highly complex and remains poorly understood. Previous work has demonstrated an important role for structural variation in a subset of cases, but the analysis lacked the resolution necessary to move beyond detection of large regions of potential interest to identification of individual genes. Autism spectrum disorders (ASDs) are common neurodevelopmental syndromes with a strong genetic component. ASDs are characterized by disturbances in social behavior, impaired verbal and nonverbal communication, as well as repetitive behaviors and/or a restricted range of interests. To identify genes likely to contribute to ASD etiology, we performed high density genotyping in 912 multiplex families from the Autism Genetics Resource Exchange (AGRE) collection and contrasted results to those obtained for 1,488 healthy controls. To enrich for variants most likely to interfere with gene function, we restricted our analyses to deletions and gains encompassing exons. Of the many genomic regions highlighted, 27 were seen to harbor rare variants in cases and not controls, both in the first phase of our analysis, and also in an independent replication cohort comprised of 859 cases and 1,051 controls. The genes identified by this method include NRXN1, a molecule in which rare ASD-related variation has been well documented by multiple groups. We find comparable support for several genes not previously implicated in the ASDs, including BZRAP1, MDGA2, CLCNKA, GRIK5 and GMPS. For each of these, mutant alleles eliminate entirely or remove the majority of protein coding sequences. Importantly, interrogation of an independently ascertained and non-overlapping ASD cohort identified eDels in these same genes in almost a third of cases, a result unlikely to occur by chance alone (p=1×10⁻³⁶ by Fisher Exact). These newly identified autism susceptibility genes will be useful in understanding key signaling pathways dysregulated in this group of disorders.

Definitions:

A “copy number variation (CNV)” refers to the number of copies of a particular gene in the genotype of an individual. CNVs represent a major genetic component of human phenotypic diversity. Susceptibility to genetic disorders is known to be associated not only with single nucleotide polymorphisms (CNV), but also with structural and other genetic variations, including CNVs. A CNV represents a copy number change involving a DNA fragment that is −1 kilobases (kb) or larger (Feuk et al. 2006 Nature. 444:444-54.). CNVs described herein do not include those variants that arise from the insertion/deletion of transposable elements (e.g., −6-kb KpnI repeats) to minimize the complexity of future CNV analyses. The term CNV therefore encompasses previously introduced terms such as large-scale copy number variants (LCVs; Iafrate et al. 2004, Nature Genetics 36: 949-51), copy number polymorphisms (CNPs; Sebat et al. 2004 Science 305:525-8.), intermediate-sized variants (ISVs; Tuzun et al. 2006 Genome Res. 16: 949-961), and eDELs, but not retroposon insertions.

A “single nucleotide polymorphism (SNP)” refers to a change in which a single base in the DNA differs from the usual base at that position. These single base changes are called SNPs or “snips.” Millions of SNPs have been cataloged in the human genome. Some SNPs such as that which causes sickle cell are responsible for disease. Other SNPs are normal variations in the genome.

A neurological disorder includes, without limitation, schizophrenia, bipolar disorder, autism, autism spectrum disorder (ASD), Tourette Syndrome, and obsessive compulsive disorder.

The term “genetic alteration” which encompasses a CNV or SNP as defined above, refers to a change from the wild-type or reference sequence of one or more nucleic acid molecules. Genetic alterations include without limitation, base pair substitutions, additions and deletions of at least one nucleotide from a nucleic acid molecule of known sequence.

The term “solid matrix” as used herein refers to any format, such as beads, microparticles, a microarray, the surface of a microtitration well or a test tube, a dipstick or a filter. The material of the matrix may be polystyrene, cellulose, latex, nitrocellulose, nylon, polyacrylamide, dextran or agarose.

The phrase “consisting essentially of when referring to a particular nucleotide or amino acid means a sequence having the properties of a given SEQ ID NO:. For example, when used in reference to an amino acid sequence, the phrase includes the sequence per se and molecular modifications that would not affect the functional and novel characteristics of the sequence.

“Target nucleic acid” as used herein refers to a previously defined region of a nucleic acid present in a complex nucleic acid mixture wherein the defined wild-type region contains at least one known nucleotide variation which may or may not be associated with neurological disorder. The nucleic acid molecule may be isolated from a natural source by cDNA cloning or subtractive hybridization or synthesized manually. The nucleic acid molecule may be synthesized manually by the triester synthetic method or by using an automated DNA synthesizer. With regard to nucleic acids used in the invention, the term “isolated nucleic acid” is sometimes employed. This term, when applied to DNA, refers to a DNA molecule that is separated from sequences with which it is immediately contiguous (in the 5′ and 3′ directions) in the naturally occurring genome of the organism from which it was derived. For example, the “isolated nucleic acid” may comprise a DNA molecule inserted into a vector, such as a plasmid or virus vector, or integrated into the genomic DNA of a prokaryote or eukaryote. An “isolated nucleic acid molecule” may also comprise a cDNA molecule. An isolated nucleic acid molecule inserted into a vector is also sometimes referred to herein as a recombinant nucleic acid molecule.

With respect to RNA molecules, the term “isolated nucleic acid” primarily refers to an RNA molecule encoded by an isolated DNA molecule as defined above. Alternatively, the term may refer to an RNA molecule that has been sufficiently separated from RNA molecules with which it would be associated in its natural state (i.e., in cells or tissues), such that it exists in a “substantially pure” form.

By the use of the term “enriched” in reference to nucleic acid it is meant that the specific DNA or RNA sequence constitutes a significantly higher fraction (2-5 fold) of the total DNA or RNA present in the cells or solution of interest than in normal cells or in the cells from which the sequence was taken. This could be caused by a person by preferential reduction in the amount of other DNA or RNA present, or by a preferential increase in the amount of the specific DNA or RNA sequence, or by a combination of the two. However, it should be noted that “enriched” does not imply that there are no other DNA or RNA sequences present, just that the relative amount of the sequence of interest has been significantly increased.

It is also advantageous for some purposes that a nucleotide sequence be in purified form. The term “purified” in reference to nucleic acid does not require absolute purity (such as a homogeneous preparation); instead, it represents an indication that the sequence is relatively purer than in the natural environment (compared to the natural level, this level should be at least 2-5 fold greater, e.g., in terms of mg/ml). Individual clones isolated from a cDNA library may be purified to electrophoretic homogeneity. The claimed DNA molecules obtained from these clones can be obtained directly from total DNA or from total RNA. The cDNA clones are not naturally occurring, but rather are preferably obtained via manipulation of a partially purified naturally occurring substance (messenger RNA). The construction of a cDNA library from mRNA involves the creation of a synthetic substance (cDNA) and pure individual cDNA clones can be isolated from the synthetic library by clonal selection of the cells carrying the cDNA library. Thus, the process which includes the construction of a cDNA library from mRNA and isolation of distinct cDNA clones yields an approximately 10⁻⁶-fold purification of the native message. Thus, purification of at least one order of magnitude, preferably two or three orders, and more preferably four or five orders of magnitude is expressly contemplated.

The term “substantially pure” refers to a preparation comprising at least 50-60% by weight the compound of interest (e.g., nucleic acid, oligonucleotide, etc.). More preferably, the preparation comprises at least 75% by weight, and most preferably 90-99% by weight, the compound of interest. Purity is measured by methods appropriate for the compound of interest.

The term “complementary” describes two nucleotides that can form multiple favorable interactions with one another. For example, adenine is complementary to thymine as they can form two hydrogen bonds. Similarly, guanine and cytosine are complementary since they can form three hydrogen bonds. Thus, if a nucleic acid sequence contains the following sequence of bases, thymine, adenine, guanine and cytosine, a “complement” of this nucleic acid molecule would be a molecule containing adenine in the place of thymine, thymine in the place of adenine, cytosine in the place of guanine, and guanine in the place of cytosine. Because the complement can contain a nucleic acid sequence that forms optimal interactions with the parent nucleic acid molecule, such a complement can bind with high affinity to its parent molecule.

With respect to single stranded nucleic acids, particularly oligonucleotides, the term “specifically hybridizing” refers to the association between two single-stranded nucleotide molecules of sufficiently complementary sequence to permit such hybridization under pre-determined conditions generally used in the art (sometimes termed “substantially complementary”). In particular, the term refers to hybridization of an oligonucleotide with a substantially complementary sequence contained within a single-stranded DNA or RNA molecule of the invention, to the substantial exclusion of hybridization of the oligonucleotide with single-stranded nucleic acids of non-complementary sequence. For example, specific hybridization can refer to a sequence which hybridizes to any neurological disorder specific marker gene or nucleic acid, but does not hybridize to other nucleotides. Also polynucleotide which “specifically hybridizes” may hybridize only to a neurospecific specific marker, such a neurological disorder-specific marker shown in the Tables contained herein. Appropriate conditions enabling specific hybridization of single stranded nucleic acid molecules of varying complementarity are well known in the art.

For instance, one common formula for calculating the stringency conditions required to achieve hybridization between nucleic acid molecules of a specified sequence homology is set forth below (Sambrook et al., Molecular Cloning, Cold Spring Harbor Laboratory (1989):

T_(m)=81.5° C.+16.6 Log [Na+]+0.41(% G+C)−0.63 (% formamide)−600/#bp in duplex

As an illustration of the above formula, using [Na+]=[0.368] and 50% formamide, with GC content of 42% and an average probe size of 200 bases, the T_(m) is 57° C. The T_(m) of a DNA duplex decreases by 1-1.5° C. with every 1% decrease in homology. Thus, targets with greater than about 75% sequence identity would be observed using a hybridization temperature of 42° C.

The stringency of the hybridization and wash depend primarily on the salt concentration and temperature of the solutions. In general, to maximize the rate of annealing of the probe with its target, the hybridization is usually carried out at salt and temperature conditions that are 20-25° C. below the calculated T_(m) of the hybrid. Wash conditions should be as stringent as possible for the degree of identity of the probe for the target. In general, wash conditions are selected to be approximately 12-20° C. below the T_(m) of the hybrid. In regards to the nucleic acids of the current invention, a moderate stringency hybridization is defined as hybridization in 6×SSC, 5×Denhardt's solution, 0.5% SDS and 100 μg/ml denatured salmon sperm DNA at 42° C., and washed in 2×SSC and 0.5% SDS at 55° C. for 15 minutes. A high stringency hybridization is defined as hybridization in 6×SSC, 5×Denhardt's solution, 0.5% SDS and 100 μg/ml denatured salmon sperm DNA at 42° C., and washed in 1×SSC and 0.5% SDS at 65° C. for 15 minutes. A very high stringency hybridization is defined as hybridization in 6×SSC, 5×Denhardt's solution, 0.5% SDS and 100 μg/ml denatured salmon sperm DNA at 42° C., and washed in 0.1×SSC and 0.5% SDS at 65° C. for 15 minutes.

The term “oligonucleotide,” as used herein is defined as a nucleic acid molecule comprised of two or more ribo- or deoxyribonucleotides, preferably more than three. The exact size of the oligonucleotide will depend on various factors and on the particular application and use of the oligonucleotide. Oligonucleotides, which include probes and primers, can be any length from 3 nucleotides to the full length of the nucleic acid molecule, and explicitly include every possible number of contiguous nucleic acids from 3 through the full length of the polynucleotide. Preferably, oligonucleotides are at least about 10 nucleotides in length, more preferably at least 15 nucleotides in length, more preferably at least about 20 nucleotides in length.

The term “probe” as used herein refers to an oligonucleotide, polynucleotide or nucleic acid, either RNA or DNA, whether occurring naturally as in a purified restriction enzyme digest or produced synthetically, which is capable of annealing with or specifically hybridizing to a nucleic acid with sequences complementary to the probe. A probe may be either single-stranded or double-stranded. The exact length of the probe will depend upon many factors, including temperature, source of probe and use of the method. For example, for diagnostic applications, depending on the complexity of the target sequence, the oligonucleotide probe typically contains 15-25 or more nucleotides, although it may contain fewer nucleotides. The probes herein are selected to be complementary to different strands of a particular target nucleic acid sequence. This means that the probes must be sufficiently complementary so as to be able to “specifically hybridize” or anneal with their respective target strands under a set of pre-determined conditions. Therefore, the probe sequence need not reflect the exact complementary sequence of the target. For example, a non-complementary nucleotide fragment may be attached to the 5′ or 3′ end of the probe, with the remainder of the probe sequence being complementary to the target strand. Alternatively, non-complementary bases or longer sequences can be interspersed into the probe, provided that the probe sequence has sufficient complementarity with the sequence of the target nucleic acid to anneal therewith specifically.

The term “primer” as used herein refers to an oligonucleotide, either RNA or DNA, either single-stranded or double-stranded, either derived from a biological system, generated by restriction enzyme digestion, or produced synthetically which, when placed in the proper environment, is able to functionally act as an initiator of template-dependent nucleic acid synthesis. When presented with an appropriate nucleic acid template, suitable nucleoside triphosphate precursors of nucleic acids, a polymerase enzyme, suitable cofactors and conditions such as a suitable temperature and pH, the primer may be extended at its 3′ terminus by the addition of nucleotides by the action of a polymerase or similar activity to yield a primer extension product. The primer may vary in length depending on the particular conditions and requirement of the application. For example, in diagnostic applications, the oligonucleotide primer is typically 15-25 or more nucleotides in length. The primer must be of sufficient complementarity to the desired template to prime the synthesis of the desired extension product, that is, to be able anneal with the desired template strand in a manner sufficient to provide the 3′ hydroxyl moiety of the primer in appropriate juxtaposition for use in the initiation of synthesis by a polymerase or similar enzyme. It is not required that the primer sequence represent an exact complement of the desired template. For example, a non-complementary nucleotide sequence may be attached to the 5′ end of an otherwise complementary primer. Alternatively, non-complementary bases may be interspersed within the oligonucleotide primer sequence, provided that the primer sequence has sufficient complementarity with the sequence of the desired template strand to functionally provide a template-primer complex for the synthesis of the extension product. Polymerase chain reaction (PCR) has been described in U.S. Pat. Nos. 4,683,195, 4,800,195, and 4,965,188, the entire disclosures of which are incorporated by reference herein.

The term “vector” relates to a single or double stranded circular nucleic acid molecule that can be infected, transfected or transformed into cells and replicate independently or within the host cell genome. A circular double stranded nucleic acid molecule can be cut and thereby linearized upon treatment with restriction enzymes. An assortment of vectors, restriction enzymes, and the knowledge of the nucleotide sequences that are targeted by restriction enzymes are readily available to those skilled in the art, and include any replicon, such as a plasmid, cosmid, bacmid, phage or virus, to which another genetic sequence or element (either DNA or RNA) may be attached so as to bring about the replication of the attached sequence or element. A nucleic acid molecule of the invention can be inserted into a vector by cutting the vector with restriction enzymes and ligating the two pieces together.

Many techniques are available to those skilled in the art to facilitate transformation, transfection, or transduction of the expression construct into a prokaryotic or eukaryotic organism. The terms “transformation”, “transfection”, and “transduction” refer to methods of inserting a nucleic acid and/or expression construct into a cell or host organism. These methods involve a variety of techniques, such as treating the cells with high concentrations of salt, an electric field, or detergent, to render the host cell outer membrane or wall permeable to nucleic acid molecules of interest, microinjection, PEG-fusion, and the like.

The term “promoter element” describes a nucleotide sequence that is incorporated into a vector that, once inside an appropriate cell, can facilitate transcription factor and/or polymerase binding and subsequent transcription of portions of the vector DNA into mRNA. In one embodiment, the promoter element of the present invention precedes the 5′ end of the neurological disorder specific marker nucleic acid molecule such that the latter is transcribed into mRNA. Host cell machinery then translates mRNA into a polypeptide.

Those skilled in the art will recognize that a nucleic acid vector can contain nucleic acid elements other than the promoter element and the neurological disorder specific marker gene nucleic acid molecule. These other nucleic acid elements include, but are not limited to, origins of replication, ribosomal binding sites, nucleic acid sequences encoding drug resistance enzymes or amino acid metabolic enzymes, and nucleic acid sequences encoding secretion signals, localization signals, or signals useful for polypeptide purification.

A “replicon” is any genetic element, for example, a plasmid, cosmid, bacmid, plastid, phage or virus, that is capable of replication largely under its own control. A replicon may be either RNA or DNA and may be single or double stranded.

An “expression operon” refers to a nucleic acid segment that may possess transcriptional and translational control sequences, such as promoters, enhancers, translational start signals (e.g., ATG or AUG codons), polyadenylation signals, terminators, and the like, and which facilitate the expression of a polypeptide coding sequence in a host cell or organism.

As used herein, the terms “reporter,” “reporter system”, “reporter gene,” or “reporter gene product” shall mean an operative genetic system in which a nucleic acid comprises a gene that encodes a product that when expressed produces a reporter signal that is a readily measurable, e.g., by biological assay, immunoassay, radio immunoassay, or by colorimetric, fluorogenic, chemiluminescent or other methods. The nucleic acid may be either RNA or DNA, linear or circular, single or double stranded, antisense or sense polarity, and is operatively linked to the necessary control elements for the expression of the reporter gene product. The required control elements will vary according to the nature of the reporter system and whether the reporter gene is in the form of DNA or RNA, but may include, but not be limited to, such elements as promoters, enhancers, translational control sequences, poly A addition signals, transcriptional termination signals and the like.

The introduced nucleic acid may or may not be integrated (covalently linked) into nucleic acid of the recipient cell or organism. In bacterial, yeast, plant and mammalian cells, for example, the introduced nucleic acid may be maintained as an episomal element or independent replicon such as a plasmid. Alternatively, the introduced nucleic acid may become integrated into the nucleic acid of the recipient cell or organism and be stably maintained in that cell or organism and further passed on or inherited to progeny cells or organisms of the recipient cell or organism. Finally, the introduced nucleic acid may exist in the recipient cell or host organism only transiently.

The term “selectable marker gene” refers to a gene that when expressed confers a selectable phenotype, such as antibiotic resistance, on a transformed cell.

The term “operably linked” means that the regulatory sequences necessary for expression of the coding sequence are placed in the DNA molecule in the appropriate positions relative to the coding sequence so as to effect expression of the coding sequence. This same definition is sometimes applied to the arrangement of transcription units and other transcription control elements (e.g. enhancers) in an expression vector.

The terms “recombinant organism,” or “transgenic organism” refer to organisms which have a new combination of genes or nucleic acid molecules. A new combination of genes or nucleic acid molecules can be introduced into an organism using a wide array of nucleic acid manipulation techniques available to those skilled in the art. The term “organism” relates to any living being comprised of a least one cell. An organism can be as simple as one eukaryotic cell or as complex as a mammal. Therefore, the phrase “a recombinant organism” encompasses a recombinant cell, as well as eukaryotic and prokaryotic organism.

The term “isolated protein” or “isolated and purified protein” is sometimes used herein. This term refers primarily to a protein produced by expression of an isolated nucleic acid molecule of the invention. Alternatively, this term may refer to a protein that has been sufficiently separated from other proteins with which it would naturally be associated, so as to exist in “substantially pure” form. “Isolated” is not meant to exclude artificial or synthetic mixtures with other compounds or materials, or the presence of impurities that do not interfere with the fundamental activity, and that may be present, for example, due to incomplete purification, addition of stabilizers, or compounding into, for example, immunogenic preparations or pharmaceutically acceptable preparations.

A “specific binding pair” comprises a specific binding member (sbm) and a binding partner (bp) which have a particular specificity for each other and which in normal conditions bind to each other in preference to other molecules. Examples of specific binding pairs are antigens and antibodies, ligands and receptors and complementary nucleotide sequences. The skilled person is aware of many other examples. Further, the term “specific binding pair” is also applicable where either or both of the specific binding member and the binding partner comprise a part of a large molecule. In embodiments in which the specific binding pair comprises nucleic acid sequences, they will be of a length to hybridize to each other under conditions of the assay, preferably greater than 10 nucleotides long, more preferably greater than 15 or 20 nucleotides long.

“Sample” or “patient sample” or “biological sample” generally refers to a sample which may be tested for a particular molecule, preferably a neurological disorder specific marker molecule, such as a marker shown in the tables provided below. Samples may include but are not limited to cells, body fluids, including blood, serum, plasma, urine, saliva, tears, pleural fluid and the like.

The terms “agent” and “test compound” are used interchangeably herein and denote a chemical compound, a mixture of chemical compounds, a biological macromolecule, or an extract made from biological materials such as bacteria, plants, fungi, or animal (particularly mammalian) cells or tissues. Biological macromolecules include siRNA, snRNA, antisense oligonucleotides, peptides, peptide/DNA complexes, and any nucleic acid based molecule which exhibits the capacity to modulate the activity of the CNV containing nucleic acids described herein or their encoded proteins. Agents are evaluated for potential biological activity by inclusion in screening assays described hereinbelow.

Methods of Using Neurological Disorder-Associated eCNVS for Diagnosing an Increased Risk for the Development of a Neurological Disorder

Neurological disorder-related-eCNV containing nucleic acids, including but not limited to those listed in the Tables provided below may be used for a variety of purposes in accordance with the present invention. Neurological disorder-associated eCNV containing DNA, RNA, or fragments thereof may be used as probes to detect the presence of and/or expression of neurological disorder specific markers. Methods in which neurological disorder specific marker nucleic acids may be utilized as probes for such assays include, but are not limited to: (1) in situ hybridization; (2) Southern hybridization (3) northern hybridization; and (4) assorted amplification reactions such as polymerase chain reactions (PCR).

Further, assays for detecting neurological disorder-associated eCNVs may be conducted on any type of biological sample, including but not limited to body fluids (including blood, CSF, urine, serum, gastric lavage), any type of cell (such as brain cells, white blood cells, mononuclear cells) or body tissue.

From the foregoing discussion, it can be seen that neurological disorder-associated eCNV containing nucleic acids, vectors expressing the same, neurological disorder eCNV containing marker proteins and anti-neurological disorder specific marker antibodies of the invention can be used to detect neurological disorder associated eCNVs in body tissue, cells, or fluid, and alter neurological disorder eCNV containing marker protein expression for purposes of assessing the genetic and protein interactions involved in the development of neurological disorder.

In most embodiments for screening for neurological disorder-associated CNVs, the neurological disorder-associated CNV containing nucleic acid in the sample will initially be amplified, e.g. using PCR, to increase the amount of the templates as compared to other sequences present in the sample. This allows the target sequences to be detected with a high degree of sensitivity if they are present in the sample. This initial step may be avoided by using highly sensitive array techniques that are becoming increasingly important in the art.

Alternatively, new detection technologies can overcome this limitation and enable analysis of small samples containing as little as 1 μg of total RNA. Using Resonance Light Scattering (RLS) technology, as opposed to traditional fluorescence techniques, multiple reads can detect low quantities of mRNAs using biotin labeled hybridized targets and anti-biotin antibodies. Another alternative to PCR amplification involves planar wave guide technology (PWG) to increase signal-to-noise ratios and reduce background interference. Both techniques are commercially available from Qiagen Inc. (USA).

Thus any of the aforementioned techniques may be used to detect or quantify neurological disorder-associated CNV marker expression and accordingly, diagnose neurological disorder(s).

Kits and Articles of Manufacture

Any of the aforementioned products can be incorporated into a kit which may contain a neurological disorder-associated CNV specific marker polynucleotide or one or more such markers immobilized on a Gene Chip, an oligonucleotide, a polypeptide, a peptide, an antibody, a label, marker, or reporter, a pharmaceutically acceptable carrier, a physiologically acceptable carrier, instructions for use, a container, a vessel for administration, an assay substrate, enzyme, or any combination thereof.

Methods of Using Neurological Disorder-Associated CNVs/SNPs Development of Therapeutic Agents

Since the CNVs identified herein have been associated with the etiology of a neurological disorder, methods for identifying agents that modulate the activity of the genes and their encoded products containing such CNVs should result in the generation of efficacious therapeutic agents for the treatment of such conditions.

As can be seen from the data provided in the Tables below, several chromosomes contain regions which provide suitable targets for the rational design of therapeutic agents which modulate their activity. Specific organic molecules can thus be identified with capacity to bind to the active site of the proteins encoded by the CNV containing nucleic acids based on conformation or key amino acid residues required for function. A combinatorial chemistry approach will be used to identify molecules with greatest activity and then iterations of these molecules will be developed for further cycles of screening. In certain embodiments, candidate agents can be screening from large libraries of synthetic or natural compounds. Such compound libraries are commercially available from a number of companies including but not limited to Maybridge Chemical Co., (Trevillet, Cornwall, UK), Comgenex (Princeton, N.J.), Microsour (New Milford, Conn.) Aldrich (Milwaukee, Wis.) Akos Consulting and Solutions GmbH (Basel, Switzerland), Ambinter (Paris, France), Asinex (Moscow, Russia) Aurora (Graz, Austria), BioFocus DPI (Switzerland), Bionet (Camelford, UK), Chembridge (San Diego, Calif.), Chem Div (San Diego, Calif.). The skilled person is aware of other sources and can readily purchase the same. Once therapeutically efficacious compounds are identified in the screening assays described herein, they can be formulated in to pharmaceutical compositions and utilized for the treatment of a neurological disorder.

The polypeptides or fragments employed in drug screening assays may either be free in solution, affixed to a solid support or within a cell. One method of drug screening utilizes eukaryotic or prokaryotic host cells which are stably transformed with recombinant polynucleotides expressing the polypeptide or fragment, preferably in competitive binding assays. Such cells, either in viable or fixed form, can be used for standard binding assays. One may determine, for example, formation of complexes between the polypeptide or fragment and the agent being tested, or examine the degree to which the formation of a complex between the polypeptide or fragment and a known substrate is interfered with by the agent being tested.

Another technique for drug screening provides high throughput screening for compounds having suitable binding affinity for the encoded polypeptides and is described in detail in Geysen, PCT published application WO 84/03564, published on Sep. 13, 1984. Briefly stated, large numbers of different, small peptide test compounds, such as those described above, are synthesized on a solid substrate, such as plastic pins or some other surface. The peptide test compounds are reacted with the target polypeptide and washed. Bound polypeptide is then detected by methods well known in the art.

A further technique for drug screening involves the use of host eukaryotic cell lines or cells (such as described above) which have a nonfunctional or altered neurological disorder associated gene. These host cell lines or cells are defective at the polypeptide level. The host cell lines or cells are grown in the presence of drug compound. The rate of neuronal signaling, ion release, or maintenance of neuronal cell morphology of the host cells is measured to determine if the compound is capable of regulating the same in the defective cells. Host cells contemplated for use in the present invention include but are not limited to bacterial cells, fungal cells, insect cells, and mammalian cells, particularly neuronal cells. The neurological disorder-associated CNV encoding DNA molecules may be introduced singly into such host cells or in combination to assess the phenotype of cells conferred by such expression. Methods for introducing DNA molecules are also well known to those of ordinary skill in the art. Such methods are set forth in Ausubel et al. eds., Current Protocols in Molecular Biology, John Wiley & Sons, NY, N.Y. 1995, the disclosure of which is incorporated by reference herein.

A wide variety of expression vectors are available that can be modified to express the novel DNA sequences of this invention. The specific vectors exemplified herein are merely illustrative, and are not intended to limit the scope of the invention. Expression methods are described by Sambrook et al. Molecular Cloning: A Laboratory Manual or Current Protocols in Molecular Biology 16.3-17.44 (1989). Expression methods in Saccharomyces are also described in Current Protocols in Molecular Biology (1989).

Suitable vectors for use in practicing the invention include prokaryotic vectors such as the pNH vectors (Stratagene Inc., 11099 N. Torrey Pines Rd., La Jolla, Calif. 92037), pET vectors (Novogen Inc., 565 Science Dr., Madison, Wis. 53711) and the pGEX vectors (Pharmacia LKB Biotechnology Inc., Piscataway, N.J. 08854). Examples of eukaryotic vectors useful in practicing the present invention include the vectors pRc/CMV, pRc/RSV, and pREP (Invitrogen, 11588 Sorrento Valley Rd., San Diego, Calif. 92121); pcDNA3.1/V5&His (Invitrogen); baculovirus vectors such as pVL1392, pVL1393, or pAC360 (Invitrogen); and yeast vectors such as YRP17, YIP5, and YEP24 (New England Biolabs, Beverly, Mass.), as well as pRS403 and pRS413 Stratagene Inc.); Picchia vectors such as pHIL-D1 (Phillips Petroleum Co., Bartlesville, Okla. 74004); retroviral vectors such as PLNCX and pLPCX (Clontech); and adenoviral and adeno-associated viral vectors.

Promoters for use in expression vectors of this invention include promoters that are operable in prokaryotic or eukaryotic cells. Promoters that are operable in prokaryotic cells include lactose (lac) control elements, bacteriophage lambda (pL) control elements, arabinose control elements, tryptophan (trp) control elements, bacteriophage T7 control elements, and hybrids thereof. Promoters that are operable in eukaryotic cells include Epstein Barr virus promoters, adenovirus promoters, SV40 promoters, Rous Sarcoma Virus promoters, cytomegalovirus (CMV) promoters, baculovirus promoters such as AcMNPV polyhedrin promoter, Picchia promoters such as the alcohol oxidase promoter, and Saccharomyces promoters such as the gal4 inducible promoter and the PGK constitutive promoter, as well as neuronal-specific platelet-derived growth factor promoter (PDGF), the Thy-1 promoter, the hamster and mouse Prion promoter (MoPrP), and the Glial fibrillar acidic protein (GFAP) for the expression of transgenes in glial cells.

In addition, a vector of this invention may contain any one of a number of various markers facilitating the selection of a transformed host cell. Such markers include genes associated with temperature sensitivity, drug resistance, or enzymes associated with phenotypic characteristics of the host organisms.

Host cells expressing the neurological disorder-associated CNVs of the present invention or functional fragments thereof provide a system in which to screen potential compounds or agents for the ability to modulate the development of neurological disorder. Thus, in one embodiment, the nucleic acid molecules of the invention may be used to create recombinant cell lines for use in assays to identify agents which modulate aspects of cellular metabolism associated with neuronal signaling and neuronal cell communication and structure. Also provided herein are methods to screen for compounds capable of modulating the function of proteins encoded by CNV containing nucleic acids.

Another approach entails the use of phage display libraries engineered to express fragment of the polypeptides encoded by the CNV containing nucleic acids on the phage surface. Such libraries are then contacted with a combinatorial chemical library under conditions wherein binding affinity between the expressed peptide and the components of the chemical library may be detected. U.S. Pat. Nos. 6,057,098 and 5,965,456 provide methods and apparatus for performing such assays.

The goal of rational drug design is to produce structural analogs of biologically active polypeptides of interest or of small molecules with which they interact (e.g., agonists, antagonists, inhibitors) in order to fashion drugs which are, for example, more active or stable forms of the polypeptide, or which, e.g., enhance or interfere with the function of a polypeptide in vivo. See, e.g., Hodgson, (1991) Bio/Technology 9:19-21. In one approach, discussed above, the three-dimensional structure of a protein of interest or, for example, of the protein-substrate complex, is solved by x-ray crystallography, by nuclear magnetic resonance, by computer modeling or most typically, by a combination of approaches. Less often, useful information regarding the structure of a polypeptide may be gained by modeling based on the structure of homologous proteins. An example of rational drug design is the development of HIV protease inhibitors (Erickson et al., (1990) Science 249:527-533). In addition, peptides may be analyzed by an alanine scan (Wells, (1991) Meth. Enzym. 202:390-411). In this technique, an amino acid residue is replaced by Ala, and its effect on the peptide's activity is determined. Each of the amino acid residues of the peptide is analyzed in this manner to determine the important regions of the peptide.

It is also possible to isolate a target-specific antibody, selected by a functional assay, and then to solve its crystal structure. In principle, this approach yields a pharmacore upon which subsequent drug design can be based.

One can bypass protein crystallography altogether by generating anti-idiotypic antibodies (anti-ids) to a functional, pharmacologically active antibody. As a mirror image of a mirror image, the binding site of the anti-ids would be expected to be an analog of the original molecule. The anti-id could then be used to identify and isolate peptides from banks of chemically or biologically produced banks of peptides. Selected peptides would then act as the pharmacore.

Thus, one may design drugs which have, e.g., improved polypeptide activity or stability or which act as inhibitors, agonists, antagonists, etc. of polypeptide activity. By virtue of the availability of CNV containing nucleic acid sequences described herein, sufficient amounts of the encoded polypeptide may be made available to perform such analytical studies as x-ray crystallography. In addition, the knowledge of the protein sequence provided herein will guide those employing computer modeling techniques in place of, or in addition to x-ray crystallography.

In another embodiment, the availability of neurological disorder-associated CNV containing nucleic acids enables the production of strains of laboratory mice carrying the neurological disorder-associated CNVs of the invention. Transgenic mice expressing the neurological disorder-associated CNV of the invention provide a model system in which to examine the role of the protein encoded by the CNV containing nucleic acid in the development and progression towards neurological disorder(s). Methods of introducing transgenes in laboratory mice are known to those of skill in the art. Three common methods include: 1. integration of retroviral vectors encoding the foreign gene of interest into an early embryo; 2. injection of DNA into the pronucleus of a newly fertilized egg; and 3. the incorporation of genetically manipulated embryonic stem cells into an early embryo. Production of the transgenic mice described above will facilitate the molecular elucidation of the role that a target protein plays in various cellular metabolic and neuronal processes. Such mice provide an in vivo screening tool to study putative therapeutic drugs in a whole animal model and are encompassed by the present invention.

The term “animal” is used herein to include all vertebrate animals, except humans. It also includes an individual animal in all stages of development, including embryonic and fetal stages. A “transgenic animal” is any animal containing one or more cells bearing genetic information altered or received, directly or indirectly, by deliberate genetic manipulation at the subcellular level, such as by targeted recombination or microinjection or infection with recombinant virus. The term “transgenic animal” is not meant to encompass classical cross-breeding or in vitro fertilization, but rather is meant to encompass animals in which one or more cells are altered by or receive a recombinant DNA molecule. This molecule may be specifically targeted to a defined genetic locus, be randomly integrated within a chromosome, or it may be extrachmmosomally replicating DNA. The term “germ cell line transgenic animal” refers to a transgenic animal in which the genetic alteration or genetic information was introduced into a germ line cell, thereby conferring the ability to transfer the genetic information to offspring. If such offspring, in fact, possess some or all of that alteration or genetic information, then they, too, are transgenic animals.

The alteration of genetic information may be foreign to the species of animal to which the recipient belongs, or foreign only to the particular individual recipient, or may be genetic information already possessed by the recipient. In the last case, the altered or introduced gene may be expressed differently than the native gene. Such altered or foreign genetic information would encompass the introduction of neurological disorder-associated CNV containing nucleotide sequences.

The DNA used for altering a target gene may be obtained by a wide variety of techniques that include, but are not limited to, isolation from genomic sources, preparation of cDNAs from isolated mRNA templates, direct synthesis, or a combination thereof.

A preferred type of target cell for transgene introduction is the embryonal stem cell (ES). ES cells may be obtained from pre-implantation embryos cultured in vitro (Evans et al., (1981) Nature 292:154-156; Bradley et al., (1984) Nature 309:255-258; Gossler et al., (1986) Proc. Natl. Acad. Sci. 83:9065-9069). Transgenes can be efficiently introduced into the ES cells by standard techniques such as DNA transfection or by retrovirus-mediated transduction. The resultant transformed ES cells can thereafter be combined with blastocysts from a non-human animal. The introduced ES cells thereafter colonize the embryo and contribute to the germ line of the resulting chimeric animal.

One approach to the problem of determining the contributions of individual genes and their expression products is to use isolated neurological disorder-associated CNV genes as insertional cassettes to selectively inactivate a wild-type gene in totipotent ES cells (such as those described above) and then generate transgenic mice. The use of gene-targeted ES cells in the generation of gene-targeted transgenic mice was described, and is reviewed elsewhere (Frohman et al., (1989) Cell 56:145-147; Bradley et al., (1992) Bio/Technology 10:534-539).

Techniques are available to inactivate or alter any genetic region to a mutation desired by using targeted homologous recombination to insert specific changes into chromosomal alleles. However, in comparison with homologous extrachromosomal recombination, which occurs at a frequency approaching 100%, homologous plasmid-chromosome recombination was originally reported to only be detected at frequencies between 10⁻⁶ and 10⁻³. Nonhomologous plasmid-chromosome interactions are more frequent occurring at levels 10⁵-fold to 10² fold greater than comparable homologous insertion.

To overcome this low proportion of targeted recombination in murine ES cells, various strategies have been developed to detect or select rare homologous recombinants. One approach for detecting homologous alteration events uses the polymerase chain reaction (PCR) to screen pools of transformant cells for homologous insertion, followed by screening of individual clones. Alternatively, a positive genetic selection approach has been developed in which a marker gene is constructed which will only be active if homologous insertion occurs, allowing these recombinants to be selected directly. One of the most powerful approaches developed for selecting homologous recombinants is the positive-negative selection (PNS) method developed for genes for which no direct selection of the alteration exists. The PNS method is more efficient for targeting genes which are not expressed at high levels because the marker gene has its own promoter. Non-homologous recombinants are selected against by using the Herpes Simplex virus thymidine kinase (HSV-TK) gene and selecting against its nonhomologous insertion with effective herpes drugs such as gancyclovir (GANC) or (1-(2-deoxy-2-fluoro-B-D arabinofluranosyl)-5-iodou-racil, (FIAU). By this counter selection, the number of homologous recombinants in the surviving transformants can be increased. Utilizing neurological disorder-associated CNV containing nucleic acid as a targeted insertional cassette provides means to detect a successful insertion as visualized, for example, by acquisition of immunoreactivity to an antibody immunologically specific for the polypeptide encoded by neurological disorder-associated CNV nucleic acid and, therefore, facilitates screening/selection of ES cells with the desired genotype.

As used herein, a knock-in animal is one in which the endogenous murine gene, for example, has been replaced with human neurological disorder-associated CNV containing gene of the invention. Such knock-in animals provide an ideal model system for studying the development of neurological disorder(s).

As used herein, the expression of a neurological disorder-associated CNV containing nucleic acid, fragment thereof, or an neurological disorder-associated CNV fusion protein can be targeted in a “tissue specific manner” or “cell type specific manner” using a vector in which nucleic acid sequences encoding all or a portion of neurological disorder-associated CNV are operably linked to regulatory sequences (e.g., promoters and/or enhancers) that direct expression of the encoded protein in a particular tissue or cell type. Such regulatory elements may be used to advantage for both in vitro and in vivo applications. Promoters for directing tissue specific proteins are well known in the art and described herein.

The nucleic acid sequence encoding the neurological disorder-associated CNV of the invention may be operably linked to a variety of different promoter sequences for expression in transgenic animals. Such promoters include, but are not limited to a prion gene promoter such as hamster and mouse Prion promoter (MoPrP), described in U.S. Pat. No. 5,877,399 and in Borchelt et al., Genet. Anal. 13(6) (1996) pages 159-163; a rat neuronal specific enolase promoter, described in U.S. Pat. Nos. 5,612,486, and 5,387,742; a platelet-derived growth factor B gene promoter, described in U.S. Pat. No. 5,811,633; a brain specific dystrophin promoter, described in U.S. Pat. No. 5,849,999; a Thy-1 promoter; a PGK promoter; a CMV promoter; a neuronal-specific platelet-derived growth factor B gene promoter; and Glial fibrillar acidic protein (GFAP) promoter for the expression of transgenes in glial cells.

Methods of use for the transgenic mice of the invention are also provided herein. Transgenic mice into which a nucleic acid containing the neurological disorder-associated CNV or its encoded protein have been introduced are useful, for example, to develop screening methods to screen therapeutic agents to identify those capable of modulating the development of neurological disorder(s).

Pharmaceuticals and Peptide Therapies

The elucidation of the role played by the neurological disorder associated CNVs described herein in neuronal signaling and brain structure facilitates the development of pharmaceutical compositions useful for treatment and diagnosis of neurological disorder(s). These compositions may comprise, in addition to one of the above substances, a pharmaceutically acceptable excipient, carrier, buffer, stabilizer or other materials well known to those skilled in the art. Such materials should be non-toxic and should not interfere with the efficacy of the active ingredient. The precise nature of the carrier or other material may depend on the route of administration, e.g. oral, intravenous, inhalation, cutaneous or subcutaneous, nasal, intramuscular, intraperitoneal routes.

Whether it is a polypeptide, antibody, peptide, nucleic acid molecule, small molecule or other pharmaceutically useful compound according to the present invention that is to be given to an individual, administration is preferably in a “prophylactically effective amount” or a “therapeutically effective amount” (as the case may be, although prophylaxis may be considered therapy), this being sufficient to show benefit to the individual.

The following materials and methods are provided to facilitate the practice of the present invention.

Sample Ascertainment

For initial screening we assembled three sample collections: 1) 943 ASD families (4,444 unique subjects) from the Autism Genetic Resource Exchange (AGRE) collection; 2) 1,070 de-identified and unrelated children of European ancestry from the Children's Hospital of Philadelphia (CHOP), with no evidence of neurological disorders; 3) 542 unrelated neurologically normal adults and seniors of European ancestry from the National Institute of Neurological Disorders and Stroke (NINDS) control collection. The AGRE families include 917 multiplex families, 24 simplex families and 2 families without an ASD diagnosis. For all analyses, AGRE cases annotated with “Autism” (n=1,463), “Broad Spectrum” (n=149) or “Not Quite Autism” (n=71) were treated equally and as affected. Samples from AGRE and NINDS were genotyped using DNA extracted from Epstein-Barr Virus (EBV)-transformed lymphoblastoid cell lines, while the CHOP controls were genotyped using DNA extracted from whole blood. All AGRE and control samples included in these analyses were genotyped on the Illumina HumanHap550 version 3 arrays, and 281 samples genotyped on version 1 arrays were excluded from the present analysis. Since the NINDS controls were genotyped at a different location and time, they were used to assess the frequency of specific CNVs in an independent cohort and to address concerns of cell line artifacts. This study was approved by the Institutional Review Board of Children's Hospital of Philadelphia. All subjects provided written informed consent for the collection of samples and subsequent analysis.

The Autism Case-Control (ACC) cohort included 859 cases from multiple sites within the United States, all of whom were of European ancestry affected with ASD. Of those, 703 were male and 156 were female; 828 met diagnostic criteria for autism, and 31 met criteria for other ASDs. Subjects ranged from 2-21 years of age when the Autism Diagnostic Interview (ADI) was given. Of the case subjects, 54% were from simplex families with the balance coming from multiplex families. The control group used for replication included 1051 children of self-reported Caucasian ancestry who had no history of ASDs. These controls were recruited by CHOP nursing and medical assistant staff under the direction of CHOP clinicians within the CHOP Health Care Network, including four primary care clinics and several group practices and outpatient practices that included well child visits.

Detection and Annotation of Copy Number Variation

For each data set, we applied identical and stringent quality control criteria to remove samples with low signal quality. CNV calls were generated using PennCNV [20], an algorithm which employs multiple sources of information, including total signal intensity, allelic intensity ratios, SNP allele frequencies, distance between neighboring SNPs, and family information to generate calls. We excluded samples meeting any of the following criteria: a) standard deviation for autosomal log R ratio values (LRR_SD) higher than 0.28, b) median B Allele Frequency (BAF_median) higher than 0.55 or lower than 0.45, c) fraction of markers with BAF values between 0.2 and 0.25 or 0.75 and 0.8 (BAF_drift) exceeded 0.002. We also excluded from our analysis CNVs within IGLC1 (22q11.22), IGHG1 (14q32.33) and IGKC (2p11.2), and the T cell receptor constant chain locus (14q11.2), as well as CNVs in chromosomes showing evidence of heterosomic aberrations (chromosome rearrangements in sub-populations of cells) in BeadStudio.

CNV calls were mapped onto genes by identifying overlap with RefSeq exons, the coordinates of which we obtained from the UCSC table browser. Deletion events overlapping with exons retrieved in this way were listed as eDels. eDups were defined as gains overlapping one or more coding exons and seen to be internal to the beginning and end of the corresponding transcript. Gains observed to encompass all exons for a given gene were annotated as gDups. P values for relative CNV burden in cases and controls were calculated at each locus by Fisher's exact test. To compare our CNV calls with other publications that have used AGRE families [10],[11],[21],[22], we examined published calls on the same individuals with the same AGRE identifiers. The CNV calls were retrieved from each corresponding publication. Quantitative PCR for CNV validationTaqMan primer/probe sets were designed to query random CNVs using FileBuilder 3.0 on the repeat-masked human genome (NCBI_(—)36; March 2006 release; http://genome.ucsc.edu/). For each assay, 10 ng of genomic DNA was assayed in quadruplicate in 10-μL reactions containing 1×final concentration TaqMan Universal Master Mix (ABI part number 4304437), and 200 nM of each primer and probe. Cycling was performed under default conditions in 384-well optical PCR plates on an ABI 7900 machine. Copy number was defined as 2-ΔΔCT, where ΔCT is the difference in threshold cycles for the sample in question normalized against an endogenous reference (RNAseP) and expressed relative to the average values obtained by three arbitrary control DNAs. A list of TaqMan probes against the 12 CNVs tested is included in Table 5.

Phylogenetic Analysis

Phylogenetic trees were estimated using the neighbor-joining algorithm, as implemented in PAUP 4.0, on an additive encoding of autosomal genotypes from one randomly selected child from 912 families.

EXAMPLE I Genome-Wide Analyses of Exonic Copy Number Variants in a Family-Based Study Point to Novel Autism Susceptibility Genes

The Autism spectrum disorders (ASDs, MIM: 209850) are a heterogeneous group of childhood diseases characterized by abnormalities in social behavior and communication, as well as patterns of restricted and repetitive behaviors[1]. Twin studies have demonstrated much higher concordance rates of ASD in monozygotic twins (92%) than dizygotic twins (10%) [2,3] indicating a strong genetic basis for autism susceptibility. Although previous work has implicated numerous genomic regions of interest [4-8], the identification of specific genetic variants that contribute to ASD risk remains challenging.

Substantial progress towards the identification of genetic risk variants has come from recent characterization of structural variation (i.e., copy number variation or CNV). For example, an initial report involving patients with syndromic autism characterized genomic variation using array comparative genomic hybridization (CGH) and identified large de novo CNVs in 28% of cases [9]. Similarly, subsequent work demonstrated that the frequency of de novo CNVs is higher in cases versus controls [7],[8]. CNV analyses have proven useful in the identification of regions that are potentially disease-related [8], [10]-[13] and have begun to be employed to advance the candidacy of individual genes, including NRXN1, CNTNAP2, and NHE9 [6], [14]-[16]. Recent work characterizing structural variation in cases and ethnically matched controls associating ubiquitin-pathway genes with autism with replicating this finding in the AGRE dataset is likewise notable [17], although family data was not reported here. Using the AGRE dataset as a discovery cohort, along with family information available for AGRE samples, we describe distinct and complementary analyses, prioritizing exonic events over CNVs in introns and intergenic intervals, which provide important new insights into the genetic architecture of the ASDs.

Towards the identification of additional genes and regions that may modulate disease risk, we have assembled a resource characterizing genome-wide structural variation from over nine hundred multiplex ASD families. Presented below are results from analyses contrasting events observed in cases and healthy ethnically matched controls, focusing on three classes of genic events: exonic deletions (eDels), exonic duplications (eDups), and whole gene duplication (gDups). Recovery of known ASD loci—together with the identification of novel regions harboring variants in multiple cases but no controls—supports the utility of this dataset. Consistent with enormous inter-individual variation, we further document a large number of events observed in only individual cases (Table 1). Importantly, all of these data have been made available to the scientific community pre-publication (on the world wide web at agre.org), greatly enhancing the utility of existing publicly accessible biomaterials and phenotype data. These data further highlight the extent of structural variation in both human and the ASDs and offer an important resource for hypothesis-generation and interrogation of individual loci.

To characterize structural variation in ASD multiplex families and unrelated controls, we typed individuals at 561,466 SNP markers using Illumina HumanHap550 version 3 arrays. After excluding samples that failed to meet QC thresholds (see Table 2), we obtained array data on 3832 individuals from 912 multiplex families enrolled in the Autism Genetic Resource Exchange (AGRE) [18], 1070 disease-free children from the Children's Hospital of Philadelphia (CHOP), and 418 neurologically normal adults and seniors from the National Institute of Neurological Disorders and Stroke (NINDS) control collection [19]. Using the PennCNV software [20], we detected CNVs with a mean size of 59.9 Kb and mean frequency of 24.3 events per individual (see Table 3). Sensitivity compares favorably with previous BAC array-based [9],[21] and SNP-based methods [8], in which mean resolution was observed to be in the range of Mbs and hundreds of Kbs, respectively.

As a first step towards validation of genotyping accuracy we examined the inheritance of CNVs in the AGRE cohort. Consistent with high quality, 96.2% of CNV calls made in children were also detected in a parent. To explore the issue of genotyping accuracy further, we generated CNV calls for an independently generated data set in which an overlapping set of 2,518 AGRE samples were genotyped using the Affymetrix 5.0 platform [11]. For CNVs (>500 kb) in known ASD regions (e.g. 15q11-13, 16p11.2, and 22q11.21; Table 4) [8],[11],[21],[22], we observed 100% correspondence between the two platforms for individuals genotyped on both platforms. For further confirmation of CNV calls, we compared de novo variants identified here to those highlighted in previous analyses of AGRE families. We identified all five de novo CNVs reported by Sebat et al [7], three of the five de novo CNVs reported by Szatmari et al [6], one de novo CNV within A2BP1 reported by Martin et al [23], and all five 16p11.2 de novo deletions reported by Weiss et al [11] and Kumar et al [10]. Of the two of thirteen de novo CNVs reported by Szatmari et al not detected as de novo in our study, one was very small (2 SNPs, 180 by on 8p23.2), and the second clearly appears to be inherited (469 SNPs, 1.4 Mb on 17p12). Thus, our data are concordant with several other studies, and provide a more comprehensive picture of de novo CNVs in multiplex autism families. To further evaluate the quality of these data on another independent platform, we used Taqman to determine relative copy number at 12 previously unreported de novo CNVs identified in AGRE probands, confirming 11/12 loci (FIG. 1 and Table 5). Together these results suggest that the CNVs calls we report are consistent and reliable.

We therefore undertook additional analyses to identify specific loci in which structural variants were enriched in cases versus controls. Because the majority of such variants were intronic or intergenic, we sought to prioritize CNVs most likely to interfere with the molecular function of specific genes. We first filtered CNV calls to include only exonic deletions (eDels) observed to overlap with a RefSeq gene. Overall, such eDels were observed at similar frequencies in AGRE cases, 1st degree relatives of AGRE cases, and unrelated controls (CHOP and NINDS cohorts), with an average of ˜2 such variants per person (Table 3). To identify events related to the ASDs we then looked for genes harboring eDels in at least one case but no unrelated controls. Among the 284 genes that met this criteria (Table 1) we observed several known ASD or mental retardation genes including: ASPM [24], DPP10 [8], CNTNAP2 [25],[26], PCDH9 [16], and NRXN1 [6]. To enrich for genes most likely to contribute to ASD risk, we used family-based calling to evaluate which of these genes carried eDels in three or more cases from at least two unrelated families (Table 6). This stringent filtering resulted in 72 genes at 55 loci, including NRXN1. This is notable, given that eleven distinct disease-linked NRXN1 variants have been identified [6],[8],[15],[27],[28]. Neurexin family members are known to interact functionally with ASD-related neuroligins [29]-[32], and likewise play an important role in synaptic specification and specialization [33],[34]. eDels in more recently identified candidates, including DPP10 and PCDH9, were likewise retained. Similarly, recovery of RNF133 and RNF148 within intron 2 of CADPS2 [7],[35] highlights additional complexity at this locus. Although CNV breakpoints cannot be mapped precisely using SNP data alone, it is possible to determine overlap with protein coding exons and use these data to predict impact on gene function. Consistent with perturbation of function, distinct alleles at the loci highlighted here are predicted to eliminate or truncate the corresponding protein products (FIG. 2).

Importantly, CNVs at a majority of these eDel loci show unique breakpoints in different families and/or result in the loss of distinct exons, demonstrating that they are independent. Moreover, because it is well established that CNVs at a subset of loci show identical breakpoints in unrelated individuals [10], this result is likely to underestimate the extent to which variants described here arose independently. Results from multi-dimensional scaling are likewise consistent with the interpretation that variants we highlight arose independently (FIG. 3).

Given the large number of variants identified, it was critically important to confirm in an independent case-control analysis, how many of these eDels were truly overrepresented in cases, as opposed to being potentially attributable to Type I error. To address this concern, we sought to determine eDel frequency in these same genes in a replication dataset comprising 859 independently ascertained ASD cases and 1051 unrelated control subjects from the Autism Case Control cohort (ACC). One third of the loci identified in the discovery phase were observed in one or more ACC controls (18/55; 32.7%), suggesting that while rare, eDels at these loci are not limited to ASD cases and family members. In contrast, and providing evidence for formal replication, 14 separate loci encompassing 22 genes were observed to carry eDels in both AGRE and ACC cases, but none of 2539 controls (Table 3). Our replication data lend strong support to the involvement of specific loci in the ASDs (Table 7). However, to ensure that these results were not observed by chance alone, we performed 10,000 permutation trials on data from the replication cohort by permuting case/control status across individuals. In each permuted dataset, we maintained the same numbers of cases and controls as in the original data, and calculated the number of genes harboring CNVs exclusively in cases. None of the 10,000 permutation trials gave results comparable to experimental observations for replicated case-specific loci (n=14; p<0.0001; FIG. 4A). In contrast, findings comparable to those for non-replicated loci (highlighted as case-specific in the discovery phase but subsequently seen in replication controls) were seen in controls in 246/10,000 trials (n=18; p=0.02; FIG. 4B).

Despite the challenges associated with obtaining statistical support for individually rare events [7],[36] we next sought to assign P values for replicated eDel loci. We were able to obtain support for each of the following loci: BZRAP1 at 17q22 (p=8.0×10⁻⁴), NRXN1 at 2p16.3 (p=3.3×10⁻⁴), MDGA2 at 14q21.3 (p=1.3×10⁻⁴), MADCAM1 at 19q13 (p=5.5×10⁻⁵), and a three gene locus at 15q11 (p=1.3×10⁻¹¹). CNV calls at each of 15q11 and 19p13 are highly-error prone, suggesting that results here be interpreted with caution (see footnotes C and F in Table 7). Recovery of NRXN1, however, provides confidence for involvement of additional loci that were likewise replicated. Benzodiazapine receptor (peripheral) associated protein 1 (BZRAP1, alternatively referred to as RIMBP1), is an adaptor molecule thought to regulate synaptic transmission by linking vesicular release machinery to voltage gated Ca2+ channels [37]. Identification of this synaptic component here, in a hypothesis-free manner, is particularly satisfying and also provides additional support for synaptic dysfunction in the ASDs [29],[38]. Less is known about MDGA2 [39], although comparison of the predicted protein to all others within GenBank by BLASTP indicated an unexpectedly high similarity to Contactin 4 (24% identity over more than 500 amino acids; Expect=3×10-39). Given previous reports of hemizygous loss of CNTN4 in individuals with mental retardation [40] and autism [17],[41], similarity between MDGA2 and CNTN4, surpassed only by resemblance to MDGA1, is notable. Likewise intriguing in light of the suggestion that common variation in cell adhesion molecules may contribute to autism risk [42] is the structural likeness of MDGA2 to members of this family of molecules. Similar results were observed for three additional genes including the Chloride Channel, Kidney, A (CLCNKA), the Kainate-Preferring Glutamate Receptor Subunit KA2 (GRIK5), and Guanine Monophosphate synthetase (GMPS) (FIG. 2); for each, eDels were identified in multiple unrelated cases, but not in any unaffected siblings or 1489 unrelated CHOP/NINDS controls (FIG. 2). Moreover, for each of these genes, at least one CNV was observed to eliminate the entire protein coding sequence. Similarly, and also consistent with perturbation of function, separate alleles identified in unrelated individuals are predicted to result in dramatically truncated proteins.

Although some published analyses emphasize the greater contribution of gene deletion events in autism pathogenesis [7], there are also clear examples of duplications that strongly modulate ASD risk [43],[44]. We therefore conducted a parallel analysis of duplications, distinguishing between events involving entire genes (gDups) which might increase dosage and those restricted to internal exons (eDups) which could give rise to a frameshift or map to a chromosomal region distinct from the reference gene. For gDups, we identified 449 genes that were duplicated in at least one AGRE case but no CHOP/NINDS controls (Table 1). Of those, 200 genes at an estimated 63 loci, including genes at 15q11.2 [43], met the more stringent criteria of being present in three or more cases from at least two independent families (Table 6). Of these, 11.5% (23/200) were also seen in ACC controls, whereas 24.5% (49/200) were case-specific in the replication cohort. Strong statistical support was obtained for established loci (e.g. p=9.3×10⁻⁶ for UBE3A and other genes in the PWS/AS region at 15q11-q13), and nominal evidence was observed for the following novel loci: CD8A at 2p11.2 (p=0.069), LOC285498 at 4p16.3 (p=0.028), and CARD9/LOC728489 at 9q34.3 (p=0.005).

For eDups, we reasoned that duplication of one or more internal exons could serve to disrupt the corresponding open reading frame and be predicted to impair gene function as a result. Despite the caveat that observed copy number gains need not map to the wild-type locus, known ASD genes including TSC2 [45] and RAH [44],[46] within the Potocki-Lupski Syndrome critical interval were amongst the 159 loci observed in at least one AGRE case, but no CHOP/NINDS controls (Table 1). Such events were also seen in one family at the NLGN1 locus, which is of interest given previous support for NLGN3 and NLGN4 [29]. Filtering of these results, using the more stringent criteria employed above in consideration of eDels, limited this set of events to 76 loci observed in at least three cases from two separate families (Table 6). Interestingly, BZRAP1, reported above to harbor eDels at significantly higher frequencies in AGRE and ACC cases versus controls (p=8.0×10⁻⁴), was amongst these, with eDups observed here in four unrelated AGRE cases (screening p=0.021). Eight other genes, including the voltage gated potassium channel subunit KCNAB2 (p=4.7×10⁻³) remained absent from ACC controls and were also replicated in the independent case cohort. Although eDups at BZRAP1 were not detected in ACC cases, eDels at this locus were replicated, underscoring the importance of variation here. When considering eDels and eDups at the BZRAP1 locus together, the likelihood of such an observation occurring by chance alone is small (p=2.3×10⁻⁵).Although none of the variants we highlight were observed in any of 2539 unrelated controls, key events, including eDels at NRXN1, BZRAP1, and MDGA2 were observed in both cases and non-autistic family members (FIG. 5). This is in keeping with previous work which suggests that haploinsufficiency at NRXN1 may contribute to the ASDs [15], but is insufficient to cause disease. Such data are also consistent with the well established finding of the “broader autism phenotype”, such as subclinical language and social impairment in first degree relatives of cases with an ASD, which supports a multi-locus model [47],[48]. We were also surprised to see that key variants at these loci appear to be transmitted to only a subset of affected individuals in some families (FIG. 5). These observations parallel findings at other major effect loci including 16p11.2 [11] and DISC1 [49],[50] and are consistent with a model in which multiple variants, common and rare, act in concert to shape clinical presentation [51]-[53]. Results are also consistent with the idea that true risk loci are likely to show incomplete penetrance and imperfect segregation with disease [13], a reality that will complicate gene finding efforts. Related to this is that substantial effort will be required to determine whether rare alleles of moderate effect act independently on distinct aspects of disease (endophenotype model) or together to undermine key processes in brain development (threshold model).

By limiting CNV calls to include only exonic deletions (eDels) and duplications (eDups and gDups), we have attempted to enrich for variants most likely to impact gene function and in doing so improve the signal to noise ratio similar to work in other complex diseases [55]. At the same time, like other gene-based strategies, we preserve our ability to consider eDels involving the same transcriptional unit as separate but equivalent. Given that such events appear rare, this is an important consideration.

Pathway analysis by DAVID [56] found support for overrepresentation of cell adhesion molecules amongst recurrent eDel genes (uncorrected p=0.002; CDH17, PCDH9, LAMA2, MADCAM1, NRXN1, POSTN, SPON2), although it should be noted that this analysis does not adjust for gene size and may favor larger genes. Nevertheless, aside from SPON2 no eDels in these genes were observed in any of the controls interrogated. In contrast, no evidence for such overrepresentation was observed for genes in the ubiquitin degradation pathway and neither term was highlighted as overrepresented amongst eDups or gDups. Given that this study focused only on events encompassing RefSeq exons, differences from Glessner and colleagues [17] are to be expected.

In summary, we have performed a high resolution genome-wide analysis to characterize the genomic landscape of copy number variation in ASDs. Through comparison of structural variation in 1,771 ASD cases and 2,539 controls and prioritization of events encompassing exons we identified more than 150 loci harboring rare variants in multiple probands but no control individuals. For each class of structural variant interrogated, the recovery of known loci serves to validate the methods employed and results obtained. Greatest confidence should be placed in loci harboring variants in multiple unrelated cases but no controls and also recovered in both screening and replication cohorts. Amongst novel genes, best support was obtained for BZRAP1 and MDGA2, intriguing candidate genes which provide novel targets for the development of therapeutics useful for the treatment of ASDs.

EXAMPLE II Screening Assays for Identifying Efficacious Therapeutics for the Treatment of Autism and ASD

The information herein above can be applied clinically to patients for diagnosing an increased susceptibility for developing autism or autism spectrum disorder and therapeutic intervention. A preferred embodiment of the invention comprises clinical application of the information described herein to a patient. Diagnostic compositions, including microarrays, and methods can be designed to identify the genetic alterations described herein in nucleic acids from a patient to assess susceptibility for developing autism or ASD. This can occur after a patient arrives in the clinic; the patient has blood drawn, and using the diagnostic methods described herein, a clinician can detect a CNV as described in Example I. The information obtained from the patient sample, which can optionally be amplified prior to assessment, will be used to diagnose a patient with an increased or decreased susceptibility for developing autism or ASD. Kits for performing the diagnostic method of the invention are also provided herein. Such kits comprise a microarray comprising at least one of the SNPs provided herein in and the necessary reagents for assessing the patient samples as described above.

The identity of autism/ASD involved genes and the patient results will indicate which variants are present, and will identify those that possess an altered risk for developing ASD. The information provided herein allows for therapeutic intervention at earlier times in disease progression than previously possible. Also as described herein above, BZRAP1, and MDGA2 provide a novel targets for the development of new therapeutic agents efficacious for the treatment of this neurological disease.

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TABLE 1 AGRE. AGRE. Cases. Screening. ACC. ACC. Cases. gene class Unrelated Controls Cases Controls Total RE.Family.ID ABCB9 gdups 3 0 0 0 5 AU1378, AU1289, AU0899, AU0836, AU0688, AU0001 ABCC1 edups 3 0 0 0 4 AU1326, AU0301, AU1534 ABHD8 gdups 2 0 0 0 2 AU2005, AU1963, AU0806 ACAT1 gdups 1 0 0 0 2 AU0022 ACP1 edels 1 0 0 0 2 AU0385 ACP6 gdups 3 0 3 0 4 AU1688, AU1610, AU1163 ACTRT1 gdups 1 0 0 0 2 AU1764 ACYP2 edels 2 0 0 1 2 AU0930, AU0381 ADAM10 gdups 1 0 0 0 2 AU0467 ADAM22 edels 1 0 0 0 2 AU1221 ADAMTS5 gdups 2 0 0 0 3 AU1416, AU1227, AU0753, AU0158 ADAMTS8 edels 2 0 0 0 2 AU0939, AU0821 ADAMTSL1 edups 2 0 0 0 3 AU1496, AU0899, AU1594 ADAMTSL2 gdups 2 0 0 0 2 AU1273, AU0897, AU0520, AU1650, AU0806 ADCK1 gdups 1 0 0 0 2 AU0755 ADCY1 edups 3 0 0 0 3 AU1486, AU1331, AU1047, AU0828, AU0196, AU0168, AU0012 ADCYAP1 gdups 1 0 0 0 2 AU0827 ADM2 gdups 4 0 0 0 4 AU1764, AU1212, AU1174, AU1164, AU0974, AU0899, AU0616, AU1944, AU1216 ADPRHL1 edels 1 0 0 0 2 AU1327 AFMID gdups 2 0 0 0 2 AU1174, AU0947, AU0991, AU0835 AGL edups 2 0 0 0 2 AU1833, AU0799, AU0771, AU0411 AHCTF1 edups 1 0 0 0 2 AU1668 AHR gdups 2 0 0 1 3 AU0440, AU0386 AK7 edels 1 0 0 0 2 AU0934 AKR1B10 edels 2 0 0 0 2 AU1145, AU0714 AKT1S1 gdups 2 0 1 0 2 AU1273, AU1072, AU0880, AU0698, AU0520, AU0068 ALDH3B2 gdups 1 0 0 0 3 AU1414, AU1228 ALKBH1 gdups 1 0 0 0 2 AU0755 ALPK3 edels 1 0 0 0 3 AU0561 AMBP gdups 1 0 0 0 2 AU0227 ANGPTL4 gdups 2 0 0 0 2 AU1592, AU1209, AU1189, AU1174, AU0899, AU0806 ANKRD41 gdups 2 0 0 0 2 AU2005, AU1963, AU0806 ANTXR2 edels 2 0 0 11 2 AU0753, AU0388, AU0114 APBA3 gdups 3 0 0 0 3 AU0520, AU0991, AU0866, AU0806 APLP1 gdups 3 0 0 0 4 AU1136, AU0599, AU0507 APOBEC3C gdups 1 0 0 0 2 AU1072, AU0550 APOBEC3D gdups 1 0 0 0 2 AU1072, AU0550 APOBEC3F gdups 1 0 0 1 2 AU1535, AU1072, AU0932, AU0550 ARHGEF16 edups 3 0 0 0 5 AU1830, AU1465, AU1412, AU1078 ARHGEF4 edels 2 0 0 0 2 AU1612, AU0991 ARID3A edups 4 0 0 0 7 AU0772, AU0725, AU0565, AU0308, AU0301, AU0139 ARIH1 edels 1 0 0 1 2 AU1309 ARL11 gdups 4 0 0 0 5 AU1056, AU0689, AU0325, AU0168, AU0055 ARRB1 edups 2 0 0 1 2 AU0430, AU0025, AU0556 ARRDC5 gdups 2 0 0 0 2 AU1912, AU1742, AU1728, AU1273, AU1193, AU1190, AU1174, AU0007, AU1527, AU0481 ARSA gdups 4 0 0 1 5 AU0794, AU0772, AU0616, AU0145, AU0051 ARSD edels 2 0 0 0 3 AU1212, AU0338 ARSD gdups 2 0 0 0 3 AU1212, AU0338, AU1625, AU0361 ARVCF gdups 4 0 4 0 4 AU1189, AU1174, AU0018, AU0991, AU0688, AU0049 ASCC3 edups 3 0 0 0 3 AU0489, AU1533, AU0982, AU0301 ASPM edels 2 0 0 1 2 AU0662, AU0176, AU0102 ATCAY gdups 3 0 0 0 3 AU0520, AU0991, AU0866, AU0806 ATP10A gdups 6 0 7 0 8 AU1331, AU0106, AU0065, AU1135, AU0385, AU0233 ATP11C edels 1 0 0 0 2 AU1823 ATP6V0D1 edups 1 0 0 0 2 AU1482, AU0700 ATP6V0D1 gdups 3 0 0 0 3 AU1207, AU0962, AU1368, AU0991, AU0835 AXUD1 gdups 1 0 0 0 2 AU1424 BAG2 edels 1 0 0 0 2 AU1215 BAI1 edups 2 0 0 0 2 AU0616, AU0568 BAIAP3 edups 1 0 0 0 2 AU1172 BBS2 gdups 1 0 0 0 2 AU1197 BC002942 gdups 5 0 0 0 6 AU1912, AU1764, AU1212, AU1174, AU1164, AU1158, AU0899, AU0616, AU1944, AU1216, AU0806 BCL9 gdups 3 0 3 0 4 AU1688, AU1610, AU1163 BCMO1 gdups 1 0 0 1 2 AU1019, AU0708 BDH1 gdups 1 0 0 0 2 AU1407, AU1087, AU0477 BGN gdups 2 0 0 0 2 AU0947, AU0897, AU0562, AU0122, AU0866 BIRC5 gdups 2 0 0 1 2 AU1174, AU0947, AU0991, AU0835 BIRC7 edups 2 0 0 0 2 AU0106, AU1915 BLOC1S2 edels 1 0 0 0 2 AU1016 BMP2K edups 1 0 0 0 2 AU1698 BNIP2 gdups 1 0 0 0 2 AU0467 BTBD2 edels 1 0 0 1 2 AU1806, AU1753 BTBD4 edups 3 0 0 0 6 AU1397, AU1273, AU0920, AU0307, AU0215 BTBD4 gdups 2 0 0 0 2 AU0939, AU0934, AU0543, AU0109 BTN2A1 edels 2 0 0 1 4 AU0561, AU0215 BTN2A3 edels 1 0 0 1 3 AU0561 BTN3A3 edels 1 0 0 1 3 AU0561 BXDC1 edels 1 0 0 1 4 AU0001 BXDC1 edups 2 0 0 0 3 AU1423, AU1341 BZRAP1 edels 6 0 2 0 8 AU1921, AU1286, AU1171, AU1105, AU0948, AU0897, AU0831, AU0803 BZRAP1 edups 4 0 0 0 4 AU1813, AU1341, AU1226, AU0899, AU0880, AU0616, AU0540, AU0085 C10orf49 edels 1 0 0 0 2 AU0305 C10orf53 gdups 2 0 0 0 2 AU0845, AU0329 C10orf72 edups 9 0 0 1 12 AU1282, AU1078, AU0994, AU0971, AU0952, AU0802, AU0698, AU0696, AU0616, AU0277, AU0134, AU0063, AU1691, AU1065 C11orf72 gdups 3 0 0 0 5 AU1414, AU1228, AU1527, AU0806 C12orf38 gdups 2 0 0 0 3 AU1007, AU0346, AU0152 C12orf49 edels 1 0 0 0 2 AU1228 C14orf151 edups 2 0 0 0 2 AU0084, AU1315 C14orf156 gdups 1 0 0 0 2 AU0755 C14orf173 edups 2 0 0 0 2 AU0084, AU1315 C15orf2 gdups 6 0 8 0 10 AU1875, AU1331, AU0744, AU0106, AU0065, AU1135, AU0233 C16orf30 gdups 2 0 0 0 2 AU0932, AU0616, AU0008, AU0688 C17orf58 gdups 1 0 0 0 2 AU1685 C19orf10 gdups 2 0 0 0 2 AU1164, AU1099, AU0947, AU0616, AU0866 C19orf15 edels 1 0 0 0 2 AU1685 C19orf19 edels 3 0 7 0 3 AU1286, AU1102, AU0995, AU1301, AU0194 C19orf20 edels 2 0 7 0 2 AU1286, AU1301, AU0194 C19orf21 edups 1 0 0 0 2 AU0022 C1GALT1 edels 1 0 0 0 2 AU0487 C1orf101 edels 1 0 0 0 2 AU0955 C1orf171 gdups 1 0 0 0 2 AU1285, AU0110 C1orf192 gdups 2 0 0 0 2 AU1875, AU1614 C1orf93 gdups 4 0 0 0 4 AU0934, AU0899, AU0880, AU0841, AU0816, AU0693, AU0520, AU0161, AU1409, AU0866, AU0481 C1QTNF1 edels 8 0 0 6 11 AU1779, AU1650, AU1338, AU1301, AU1292, AU1286, AU0951, AU0932, AU0598, AU1332, AU1107, AU0903, AU0803 C20orf141 gdups 2 0 0 0 2 AU1391, AU0758, AU0752, AU0509, AU0111, AU0049, AU0790 C20orf151 edels 2 0 0 20 2 AU1231, AU1318, AU0803 C20orf72 gdups 1 0 0 0 2 AU1520 C21orf34 edups 1 0 0 0 2 AU0799 C21orf51 gdups 3 0 0 2 4 AU1510, AU1233, AU1227, AU1213, AU0753, AU0747, AU0661, AU1213, AU0158 C21orf70 gdups 2 0 0 0 2 AU1227, AU1039, AU0753, AU0158 C22orf25 gdups 3 0 4 0 3 AU0520, AU0018, AU0991, AU0049 C22orf29 gdups 3 0 4 0 3 AU0018, AU0991, AU0049 C6orf107 gdups 2 0 0 1 2 AU1575, AU1412, AU0668 C6orf213 edels 1 0 0 0 2 AU0880 C6orf65 edels 1 0 0 0 3 AU1533 C7orf20 gdups 1 0 0 0 2 AU0385 C7orf27 gdups 2 0 0 0 2 AU0555, AU0806 C8orf74 edels 1 0 0 0 2 AU1171 C9orf28 edups 2 0 0 0 4 AU1255, AU0780, AU0352 C9orf48 edels 1 0 0 1 2 AU0535 C9orf7 gdups 2 0 0 0 2 AU1273, AU0897, AU0520, AU1650, AU0806 C9orf90 gdups 2 0 0 0 2 AU1174, AU0866, AU0835 CA5A edups 3 0 0 0 3 AU0565, AU0308, AU0820 CA6 edels 3 0 1 0 3 AU1907, AU1226, AU0314 CABLES2 edels 2 0 0 19 2 AU1231, AU1318, AU0803 CACHD1 edups 3 0 0 0 5 AU0285, AU0029, AU1224 CACNA2D2 edups 1 0 0 0 2 AU1189, AU0178 CACNA2D4 edups 5 0 0 0 5 AU1551, AU1234, AU1072, AU0947, AU0263, AU0991 CALB2 gdups 1 0 0 0 2 AU1551 CALCR edels 2 0 0 0 2 AU1212, AU0049 CAND2 edels 2 0 0 0 3 AU1377, AU0025 CARD11 edups 3 0 0 1 4 AU1427, AU1328, AU1298 CARD9 gdups 5 0 1 0 5 AU1197, AU1072, AU0947, AU0934, AU0897, AU1283, AU1216, AU1033, AU0991, AU0068 CASQ2 gdups 1 0 0 0 2 AU0651 CBLN3 gdups 4 0 0 0 5 AU0980, AU0974, AU0742, AU0568, AU0551, AU0399 CBR1 gdups 2 0 0 0 3 AU1227, AU0753, AU0316, AU0158 CCDC3 edels 1 0 0 0 2 AU0305 CCDC46 edels 2 0 0 1 2 AU0742, AU0452, AU0121, AU0051 CCDC65 edups 1 0 0 0 2 AU1353 CCDC67 edels 1 0 0 0 2 AU1261 CCDC94 gdups 2 0 0 0 2 AU1164, AU1099, AU0947, AU0934, AU0991 CCL1 gdups 1 0 0 1 2 AU1559, AU0018 CCL11 gdups 1 0 0 1 2 AU1559, AU0018 CCL13 gdups 2 0 0 3 3 AU1559, AU0450, AU0018 CCL14 gdups 1 0 0 0 2 AU0806 CCL15 gdups 1 0 0 0 2 AU0806 CCL18 gdups 1 0 0 0 2 AU0806 CCL2 gdups 1 0 0 1 2 AU1559, AU0018 CCL23 gdups 1 0 0 0 2 AU0806 CCL3 edels 1 0 0 0 2 AU1551 CCL7 gdups 1 0 0 1 2 AU1559, AU0018 CCL8 gdups 1 0 0 1 2 AU1559, AU0018 CCNB2 gdups 1 0 0 0 2 AU0467 CCRK edels 1 0 0 0 2 AU1516 CD8A gdups 2 0 1 0 3 AU1338, AU0600 CDC42EP4 edels 1 0 0 0 2 AU1921, AU1301 CDC45L gdups 3 0 4 0 3 AU0018, AU0991, AU0049 CDC5L edups 1 0 0 0 3 AU1867 CDH17 edels 2 0 0 0 3 AU0938, AU0355 CDK5RAP2 edups 1 0 0 0 2 AU0993, AU0076 CDK9 gdups 2 0 0 0 2 AU1174, AU1164, AU0932, AU0298, AU1650 CDR1 edels 1 0 0 0 2 AU1823 CDRT15 edels 1 0 0 1 2 AU0149 CDRT15 gdups 1 0 0 0 2 AU0707 CDRT4 edels 1 0 0 1 2 AU0149 CDRT4 gdups 1 0 0 0 2 AU0707 CEBPA gdups 3 0 0 1 3 AU1273, AU0934, AU0897, AU1963, AU1216, AU0991 CEL gdups 2 0 0 0 2 AU0698, AU0866 CELSR1 edups 6 0 0 0 7 AU1778, AU0688, AU0627, AU0540, AU0371, AU0307, AU1728, AU1527 CENPT gdups 3 0 0 0 4 AU0647, AU1368, AU1055 CENTA1 gdups 1 0 0 0 2 AU0385 CERK edups 3 0 0 0 5 AU0932, AU0816, AU0467, AU1610, AU0068 CERK gdups 5 0 0 0 5 AU1963, AU1527, AU1216, AU0806, AU0481 CGB gdups 1 0 0 3 2 AU1088 CGB1 gdups 2 0 0 2 3 AU1088, AU0698 CGB2 gdups 2 0 0 2 3 AU1088, AU0698 CGB5 gdups 2 0 0 2 3 AU1088, AU0698 CGB8 gdups 2 0 0 2 3 AU1088, AU0698 CGI-38 gdups 3 0 0 0 3 AU1207, AU0962, AU1368, AU0991, AU0835 CHD1L gdups 2 0 3 0 3 AU1610, AU1163, AU1688 CHD9 edups 2 0 1 0 3 AU1558, AU1511 CHIC2 edels 2 0 0 0 2 AU0533, AU1333, AU0779 CHODL edels 1 0 0 0 2 AU0276 CHRNA4 edels 1 0 0 0 2 AU1921, AU0033 CHRNA4 gdups 2 0 0 0 2 AU1174, AU0932, AU0693, AU0678, AU0520, AU0991, AU0806 CHRNG gdups 1 0 0 0 2 AU1213, AU0520 CHST3 gdups 1 0 0 0 2 AU0862 CLCN7 edups 1 0 0 0 2 AU1990, AU1806 CLCNKA edels 4 0 0 0 4 AU1875, AU1048, AU0106, AU1944 CLDN17 gdups 2 0 0 0 3 AU1227, AU0816, AU0753, AU0158 CLDN5 gdups 3 0 4 0 3 AU0018, AU0991, AU0049 CLDN6 edels 2 0 4 0 2 AU1085, AU1338, AU1107 CLDN8 gdups 2 0 0 0 3 AU1227, AU0816, AU0753, AU0158 CLDN9 edels 2 0 4 0 2 AU1085, AU1338, AU1107 CLEC2D edups 1 0 0 0 2 AU1444 CLEC4G gdups 1 0 0 0 2 AU1730 CLTCL1 gdups 3 0 4 0 3 AU0018, AU0991, AU0049 CNNM1 edels 1 0 0 0 2 AU0325 CNTNAP2 edels 2 0 0 0 2 AU0880, AU0193 COG4 gdups 1 0 0 0 2 AU1551, AU0686 COL16A1 edups 5 0 0 1 6 AU1594, AU1158, AU0980, AU0763, AU0689, AU0258, AU0110, AU1283, AU0835 COL20A1 edels 1 0 0 3 2 AU1921, AU0033 COL20A1 edups 1 0 0 0 2 AU0325 COL20A1 gdups 2 0 0 0 2 AU1174, AU0932, AU0693, AU0678, AU0520, AU0991, AU0806 COL22A1 edups 1 0 0 0 3 AU0430 COL27A1 edels 2 0 0 1 4 AU1301, AU0489 COL6A1 edups 2 0 0 0 2 AU1764, AU0991 COMT gdups 3 0 4 0 3 AU0018, AU0991, AU0049 COQ7 gdups 1 0 0 0 2 AU0993 CORO7 gdups 4 0 0 0 5 AU1742, AU1212, AU1207, AU1174, AU1164, AU0971, AU0947, AU0899, AU0830, AU0688, AU0678, AU0081, AU1963 COX10 edels 1 0 0 1 2 AU0149 COX4I1 gdups 3 0 0 0 4 AU0920, AU0298, AU0179 CPNE5 edups 2 0 0 0 2 AU0905, AU1230 CPNE7 edups 3 0 0 0 4 AU1417, AU0795, AU0777, AU1921 CPS1 edels 1 0 0 0 2 AU0717 CPXM2 edups 2 0 0 0 2 AU1215, AU0053 CREB3L3 gdups 9 0 0 0 9 AU1099, AU0991, AU0947, AU0934, AU0911, AU0897, AU0241, AU0206, AU1527, AU0866, AU0742, AU0688, AU0676 CRELD2 gdups 3 0 0 0 3 AU1742, AU1368, AU1174, AU1055, AU0932, AU0916, AU0520, AU0991 CRYGA gdups 1 0 0 0 2 AU1060 CRYZ gdups 1 0 0 0 2 AU1285, AU0110 CSAG2 gdups 1 0 0 0 2 AU1439, AU0254 CSAG3B gdups 1 0 0 0 2 AU1439, AU0254 CSTF2T gdups 2 0 0 0 3 AU0640, AU0329 CT45-5 gdups 2 0 0 0 2 AU0542, AU0080 CT45-6 gdups 2 0 0 0 2 AU0542, AU0080 CWF19L1 edels 1 0 0 0 2 AU1016 CXorf40A gdups 1 0 0 0 2 AU0308 CYB5R2 gdups 1 0 0 0 2 AU1309 CYBASC3 gdups 2 0 0 0 3 AU1323, AU0918 CYP2B6 edels 2 0 0 1 2 AU1486, AU1317 CYP4A11 gdups 1 0 0 1 3 AU0052 CYP4A22 gdups 2 0 0 0 4 AU1550, AU0052 CYP4F22 edels 3 0 0 2 4 AU1685, AU1411, AU1171, AU1157, AU1069 CYP4X1 gdups 2 0 0 0 4 AU1550, AU0052 CYP4Z1 gdups 2 0 0 0 4 AU1550, AU0052 DAB1 edels 1 0 0 0 2 AU0325 DACH1 edels 8 0 0 7 10 AU0265, AU0250, AU0210, AU0208, AU0203, AU0179, AU0173, AU0108, AU0102, AU0098, AU0056, AU0820, AU0134, AU0123 DACT2 gdups 1 0 0 0 2 AU1409 DAK gdups 4 0 0 0 6 AU1728, AU1323, AU1215, AU1009, AU0995, AU0918, AU0658, AU0262 DAPK3 gdups 7 0 0 0 7 AU1273, AU1193, AU1189, AU1164, AU1137, AU1072, AU0947, AU0932, AU0520, AU1216, AU0991, AU0866, AU0806, AU0688 DAZAP1 gdups 8 0 0 0 8 AU1778, AU1632, AU1368, AU1353, AU1277, AU1212, AU1207, AU1174, AU1164, AU0974, AU0939, AU0934, AU0924, AU0899, AU0883, AU0795, AU0753, AU0081, AU1944, AU1527, AU1033, AU0866, AU0835 DBH edups 2 0 0 0 3 AU1695, AU1536, AU1289 DCUN1D2 edels 1 0 0 0 2 AU1327 DDB1 gdups 3 0 0 0 4 AU1728, AU1323, AU1215, AU1009, AU0995, AU0658, AU0262 DDX19A gdups 1 0 0 0 2 AU1551, AU1445, AU0686 DDX19B gdups 1 0 0 0 2 AU1551, AU1445, AU0686 DEFB125 gdups 2 0 0 0 2 AU1534, AU1322 DGCR14 gdups 3 0 4 0 3 AU0018, AU0991, AU0049 DGCR2 gdups 3 0 4 0 3 AU0018, AU0991, AU0049 DGCR6L gdups 2 0 3 0 2 AU0018, AU0049 DGCR8 gdups 3 0 4 0 3 AU0520, AU0018, AU0991, AU0049 DGKB edels 8 0 0 0 10 AU1400, AU1185, AU1074, AU0953, AU0767, AU0688, AU0399, AU0178, AU0110, AU1368, AU0289 DHTKD1 gdups 1 0 0 3 2 AU0032 DHX29 edels 3 0 0 1 3 AU1823, AU1616, AU1054, AU0242 DHX34 edels 1 0 0 1 2 AU1685 DIDO1 edups 2 0 0 0 2 AU0506, AU0099 DIDO1 gdups 4 0 0 0 4 AU0467, AU0099, AU0835, AU0676, AU0210 DKFZP686A10121 edels 2 0 0 3 3 AU0049, AU0030 DKFZP686E2158 gdups 1 0 0 0 2 AU0293 DLGAP1 edels 4 0 0 0 5 AU1069, AU0952, AU0509, AU0453, AU0055, AU0052, AU0043 DNAJC10 edels 2 0 0 1 2 AU1798, AU0839, AU0134 DNAJC15 edups 1 0 0 1 2 AU0043 DNAJC17 edups 7 0 0 0 13 AU1587, AU1399, AU1377, AU1211, AU1178, AU0958, AU0165 DOCK6 gdups 4 0 0 0 4 AU1193, AU1174, AU1164, AU0962, AU0934, AU0899, AU0520, AU0122, AU0991, AU0796 DOT1L gdups 2 0 0 0 2 AU0991, AU0947, AU0298, AU0806, AU0676 DPP10 edels 2 0 0 0 3 AU0543, AU0465 DSCR1 gdups 3 0 0 2 4 AU1510, AU1233, AU1227, AU1213, AU0753, AU0747, AU0661, AU1213, AU0158 DTX1 edels 1 0 0 1 2 AU1171 DTX2 gdups 2 0 0 2 2 AU1632, AU0352, AU0314, AU0085 DUSP13 edups 2 0 0 0 3 AU1327, AU1289, AU0085 DUSP7 gdups 1 0 0 0 2 AU1190 E2F4 gdups 12 0 0 0 16 AU0939, AU0899, AU0610, AU0509, AU0450, AU0210, AU0028, AU1368, AU0991, AU0835 EBI3 gdups 2 0 0 0 2 AU1164, AU1099, AU0947, AU0934, AU0991 EDG5 gdups 3 0 0 0 3 AU1764, AU1174, AU1164, AU1963, AU0796 EDG6 gdups 2 0 0 0 2 AU1277, AU1174, AU0947, AU0622, AU0081, AU1534 EDG8 gdups 2 0 1 0 2 AU1273, AU1174, AU1164, AU0701, AU0866 EEF2 gdups 7 0 0 0 7 AU1273, AU1193, AU1189, AU1164, AU1137, AU1072, AU0947, AU0932, AU0520, AU1216, AU0991, AU0866, AU0806, AU0688 EEFSEC gdups 1 0 0 0 2 AU0835 EFHA2 edels 2 0 0 0 3 AU1470, AU0477 EFHB edups 1 0 0 0 2 AU0897 ELMO3 gdups 12 0 0 0 16 AU0939, AU0899, AU0610, AU0509, AU0450, AU0210, AU0028, AU1368, AU0991, AU0835 ELP4 edels 2 0 0 7 3 AU0905, AU0117, AU0290 EPHA10 edups 1 0 0 0 2 AU0616 EPRS edels 2 0 0 0 3 AU1344, AU0053 EPX edups 1 0 0 0 2 AU0257 ERAS gdups 1 0 0 0 2 AU1465 ERGIC1 edups 4 0 0 0 5 AU1368, AU1289, AU0899, AU0781 ESPN edels 1 0 0 8 2 AU1612, AU1301 EYA4 edups 1 0 0 0 2 AU1324 F2RL2 edels 1 0 0 0 3 AU0980, AU0301 F9 edels 1 0 0 0 2 AU1823 FABP3 edels 1 0 0 0 3 AU0700 FAM102A gdups 2 0 0 0 2 AU1174, AU0934, AU0866, AU0835 FAM110C edels 1 0 0 0 2 AU0385 FAM18B2 edels 1 0 0 1 2 AU0149 FAM18B2 gdups 1 0 0 0 2 AU0707 FAM19A1 edels 1 0 1 0 2 AU0034 FAM19A4 edels 1 0 1 0 2 AU0034 FAM20C gdups 1 0 0 0 2 AU0385 FAM21B gdups 2 0 0 1 2 AU1713, AU0845, AU0329 FAM43A gdups 1 0 0 0 2 AU0568 FAM81A gdups 1 0 0 0 2 AU0467, AU0236 FAM89B edels 3 0 1 0 4 AU1520, AU1439, AU1102 FANCL edups 1 0 0 0 2 AU1299, AU1296 FARSA edups 1 0 0 0 2 AU0599 FBXL8 gdups 1 0 0 0 2 AU0962, AU0210 FCER2 gdups 1 0 0 0 2 AU1730 FGF13 edels 1 0 0 0 2 AU1823 FGR edels 1 0 0 0 2 AU1798 FGR gdups 2 0 0 0 2 AU0783, AU0450, AU0085, AU0043, AU0008, AU1284 FHOD1 gdups 13 0 0 0 18 AU0939, AU0899, AU0722, AU0610, AU0509, AU0450, AU0210, AU0028, AU1368, AU0991, AU0899, AU0835 FKSG24 gdups 3 0 0 0 3 AU1277, AU1174, AU0947, AU0520, AU0991, AU0866 FLJ10379 gdups 2 0 0 2 3 AU1067, AU0821, AU0705, AU0640 FLJ11171 gdups 1 0 0 0 2 AU1551 FLJ11331 edels 1 0 0 6 2 AU1275, AU0603, AU0556 FLJ12529 edups 6 0 0 0 12 AU1909, AU1640, AU1563, AU1327, AU1261, AU1072, AU0922, AU0199, AU0917 FLJ12949 edups 9 0 0 0 13 AU1406, AU1172, AU0920, AU0722, AU0689, AU0648, AU0629, AU0310, AU1187, AU1033, AU0806 FLJ14668 gdups 3 0 0 0 4 AU0722, AU0465, AU0149, AU0051 FLJ20323 edels 1 0 0 0 2 AU1105, AU0150 FLJ20487 gdups 1 0 0 0 2 AU0786 FLJ21865 edels 3 0 0 9 3 AU1779, AU1650, AU1286, AU1240, AU1332, AU0803 FLJ22671 edups 1 0 0 0 2 AU1244 FLJ22688 gdups 2 0 1 0 2 AU1273, AU1072, AU0980, AU0880, AU0830, AU0753, AU0520, AU0068 FLJ25416 edels 1 0 0 0 2 AU1523, AU0246 FLJ25976 gdups 1 0 0 0 2 AU0755 FLJ37440 edups 1 0 0 0 3 AU1536, AU1163 FLJ38991 gdups 3 0 0 0 5 AU1462, AU1039, AU0551 FLJ41603 edups 3 0 0 0 5 AU1652, AU1486, AU1443, AU1389, AU0028 FLJ41993 gdups 3 0 0 0 3 AU1742, AU1368, AU1174, AU1055, AU0932, AU0916, AU0520, AU0991 FLJ43860 edups 3 0 0 0 3 AU1695, AU1374, AU1342, AU1102, AU0903, AU0763 FLJ44815 gdups 1 0 0 1 2 AU1559, AU0018 FLJ44894 edels 2 0 0 7 4 AU1559, AU1266, AU0686, AU0493, AU0208, AU0030 FLJ45831 edels 1 0 0 1 2 AU0149 FLJ45831 gdups 1 0 0 0 2 AU0707 FLJ45850 gdups 2 0 0 0 2 AU1174, AU0934, AU0816, AU1527, AU0481 FLRT1 gdups 6 0 0 0 6 AU0962, AU0947, AU0934, AU1164, AU1033, AU0866, AU0835, AU0806, AU0796 FLYWCH1 edels 3 0 3 0 3 AU1601, AU1338, AU1107 FMO5 gdups 2 0 3 0 3 AU1688, AU1610, AU1163 FRMD3 edups 2 0 0 0 2 AU1043, AU0897 FRMD4A edels 1 0 0 0 2 AU0241 FRMD4A edups 1 0 0 0 2 AU1806 FUK gdups 1 0 0 0 2 AU1551, AU0686 FUT10 edups 3 0 0 0 4 AU0788, AU0752, AU0618, AU0800 GABRA5 gdups 5 0 7 0 8 AU1331, AU0106, AU0065, AU1135, AU0233 GABRB3 gdups 6 0 8 0 9 AU1331, AU0106, AU0065, AU1135, AU0385, AU0233 GABRG3 gdups 5 0 6 0 8 AU1331, AU0106, AU0065, AU1135, AU0233 GAK gdups 2 0 1 0 2 AU1164, AU0947, AU0806 GALNT13 edels 4 0 1 0 6 AU1509, AU1185, AU0781, AU0692, AU0653, AU0481, AU0481, AU0125 GAMT gdups 8 0 0 0 8 AU1778, AU1632, AU1368, AU1353, AU1277, AU1212, AU1207, AU1174, AU1164, AU0974, AU0939, AU0934, AU0924, AU0899, AU0883, AU0795, AU0753, AU0081, AU1944, AU1527, AU1368, AU1212, AU1164, AU1033, AU0866, AU0835 GATA1 gdups 1 0 0 0 2 AU1465 GBGT1 gdups 2 0 0 0 2 AU1164, AU0916, AU0899, AU0520, AU1368 GCNT3 gdups 1 0 0 0 2 AU0467 GDPD4 edups 1 0 0 0 2 AU1525 GEMIN4 edups 2 0 0 0 3 AU0662, AU0164 GGN edels 1 0 0 0 2 AU1685 GGN gdups 4 0 0 0 5 AU1685, AU1273, AU0680, AU0618, AU0379, AU0325, AU0001, AU0796 GIMAP4 edels 2 0 0 0 2 AU0257, AU0162 GIMAP6 edels 2 0 0 0 2 AU0257, AU0162 GJA8 gdups 3 0 1 0 4 AU1688, AU1610, AU1163 GLT25D1 edups 1 0 0 0 2 AU1429, AU1075 GMPS edels 3 0 0 0 4 AU1221, AU0714, AU0825 GNA11 gdups 6 0 0 0 6 AU2005, AU1652, AU1174, AU1164, AU1072, AU0081, AU1963, AU1944, AU0481 GNB1L gdups 3 0 4 0 3 AU0018, AU0991, AU0049 GNG7 edups 2 0 1 0 3 AU1632, AU0289, AU0109, AU0796 GOLGA8B gdups 1 0 0 0 2 AU1031, AU0656 GOLGA8E gdups 2 0 0 0 3 AU1331, AU0106 GPR146 gdups 2 0 0 1 3 AU1212, AU1174, AU0385, AU0806 GPR17 gdups 1 0 0 0 2 AU1327, AU1174, AU1099, AU0920, AU0836 GPR30 gdups 1 0 0 0 2 AU1174, AU0385 GPR89A gdups 3 0 1 0 4 AU1688, AU1610, AU1163 GRIK5 edels 3 0 0 5 4 AU0862, AU1305, AU1286 GRIP2 edups 2 0 0 0 2 AU1190, AU1072 GSCL gdups 3 0 4 0 3 AU0018, AU0991, AU0049 GSTP1 gdups 1 0 0 0 3 AU1414, AU1228 GTF2A2 gdups 1 0 0 0 2 AU0467 GUCA1C edups 1 0 0 0 2 AU0238 GYG2 edels 2 0 0 0 4 AU1059, AU0338 GYG2 gdups 2 0 0 0 3 AU1212, AU0338, AU1625, AU0361 GYPE edels 1 0 0 1 2 AU1822 HAMP edels 1 0 0 0 2 AU1553, AU1301 HCFC1R1 edels 2 0 1 0 2 AU1085, AU1338, AU1107 HDAC6 gdups 1 0 0 0 2 AU1465 HDCMA18P edels 1 0 0 4 2 AU1275, AU0603, AU0556 HEATR2 gdups 1 0 0 0 2 AU0385 HECA edups 1 0 0 0 3 AU1830 HES7 gdups 11 0 0 0 17 AU0991, AU0947, AU0939, AU0883, AU0880, AU0616, AU0520, AU0399, AU1283, AU0250, AU0169 HEXA edels 1 0 0 0 2 AU1427 HFM1 edels 2 0 0 0 2 AU0991, AU1619 HIRA gdups 3 0 4 0 3 AU0018, AU0991, AU0049 HM13 gdups 2 0 0 0 2 AU1694, AU0952 HMGN3 edels 1 0 0 0 2 AU1009 HNF4G edels 2 0 0 0 3 AU0745, AU0604, AU1212 HOXA1 gdups 1 0 0 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AU1137 OR5D18 edels 1 0 0 2 2 AU1240, AU1137 OR5H6 gdups 1 0 0 1 2 AU1622 OR5L1 edels 1 0 0 2 2 AU1240, AU1137 OR5L2 edels 1 0 0 2 2 AU1240, AU1137 OR6F1 edels 2 0 0 0 2 AU1368, AU0951 OSBPL11 gdups 1 0 0 0 2 AU0911 OSBPL5 edups 4 0 0 0 4 AU1764, AU1277, AU1072, AU1944, AU1368, AU1216 OTOP2 gdups 2 0 0 0 2 AU0298, AU0806 OTOR gdups 2 0 1 0 2 AU1158, AU1143 OTUD5 gdups 1 0 0 0 2 AU1465 OVCH2 gdups 1 0 0 0 2 AU1309 OVOL2 gdups 1 0 0 0 2 AU1520 OXSR1 edups 2 0 0 0 2 AU1512, AU1274, AU1094, AU0991 PAMCI edels 2 0 0 0 3 AU0802, AU0325, AU0028 PAQR4 edels 3 0 4 0 3 AU1921, AU1601, AU10851, AU1338, AU1107 PARD3B edels 1 0 0 2 2 AU0733 PCDH15 edels 2 0 0 0 2 AU0783, AU0465, AU0043, AU0599 PCDH9 edels 2 0 0 0 4 AU0753, AU0482, AU0109 PCMTD2 edels 1 0 0 0 2 AU0729 PCQAP gdups 3 0 3 0 3 AU1334, AU0018, AU1334, AU0049, AU0018 PCSK1N gdups 1 0 0 0 2 AU1465 PDE4A edups 2 0 0 0 2 AU1067, AU0467 PDE4A gdups 2 0 1 0 2 AU1663, AU1273, AU1174, AU1164, AU0701, AU0866 PDE4C gdups 2 0 0 0 2 AU1277, AU1174, AU0947, AU0520, AU0991 PDE4DIP gdups 1 0 0 2 4 AU0700, AU0167 PDE5A edups 2 0 0 0 2 AU1172, AU0803, AU1105 PDE8A edels 1 0 0 0 3 AU0561 PDGFA gdups 1 0 0 0 2 AU0385 PDGFD edels 1 0 0 0 2 AU1211 PEMT gdups 2 0 0 1 2 AU1164, AU0806 PFN2 edels 2 0 0 0 2 AU0707, AU0686, AU0548 PHF2 edups 2 0 0 0 2 AU1368, AU1650 PHKB edels 2 0 0 0 2 AU1713, AU1171, AU0687 PHYH edels 1 0 0 0 2 AU0305 PI4KA gdups 3 0 4 0 3 AU1334, AU0049, AU0018 PIK3C2G edups 1 0 0 2 2 AU1798 PIK3R2 gdups 5 0 0 0 5 AU1277, AU1197, AU1174, AU0947, AU0520, AU0991, AU0866, AU0795 PIM2 gdups 1 0 0 0 2 AU1465 PIM3 gdups 3 0 0 0 3 AU1742, AU1368, AU1174, AU1055, AU0932, AU0916, AU0520, AU0991 PIP5K1C gdups 7 0 0 0 7 AU1189, AU1164, AU1072, AU0897, AU0614, AU0520, AU1944, AU1527, AU0991, AU0866, AU0806 PIWIL2 edups 1 0 0 0 2 AU0199 PKD1L2 gdups 1 0 0 1 2 AU1019, AU0708 PKD2L1 edels 1 0 0 0 2 AU1016 PKIB edels 1 0 0 0 2 AU1031 PKMYT1 edels 3 0 4 0 3 AU1921, AU1085, AU1601, AU1338, AU1107 PLA2G4C edups 2 0 0 0 3 AU1088, AU0393 PLCB1 edels 1 0 0 0 2 AU1368 PLD4 gdups 2 0 0 0 2 AU0008, AU1055 PLEKHA9 edels 1 0 0 0 2 AU0088 PLEKHG4 gdups 12 0 0 0 16 AU0939, AU0899, AU0875, AU0610, AU0450, AU0210, AU0028, AU1368, AU0991, AU0835 PLEKHG5 edels 1 0 0 8 2 AU1301 PLEKHG5 edups 4 0 0 0 7 AU1587, AU0725, AU0455, AU0020 PLEKHM2 edels 3 0 0 2 3 AU1185, AU0932, AU0063, AU1030, AU0319 PLVAP gdups 2 0 0 0 2 AU2005, AU1626, AU1963, AU0481 PMP22 edels 1 0 0 1 2 AU0149 PMP22 gdups 1 0 0 0 2 AU0707 PNKP gdups 2 0 1 0 2 AU1273, AU1072, AU0880, AU0698, AU0520, AU0068 PNLIPRP1 edels 2 0 0 0 2 AU0977, AU0819 PNPLA7 gdups 1 0 0 0 2 AU1650 PODN gdups 1 0 0 0 2 AU1811 POSTN edels 3 0 0 0 4 AU1409, AU0875, AU0600, AU0246 PP2447 edups 5 0 0 0 7 AU1833, AU1822, AU1582, AU1494, AU1424, AU1364, AU1348, AU1300, AU0231, AU0169, AU1861 PP2447 gdups 8 0 0 0 8 AU0897, AU0693, AU0688, AU0520, AU1216, AU0991, AU0866, AU0722 PPFIBP2 gdups 1 0 0 0 2 AU1309 PPME1 edups 4 0 0 0 6 AU1939, AU1862, AU1713, AU1532, AU1389, AU1271 PPP1R12C edels 1 0 0 1 2 AU1301 PQBP1 gdups 1 0 0 0 2 AU1465 PRB3 edels 3 0 0 0 7 AU1516, AU1423, AU1008, AU0951, AU0828 PRDM10 edups 3 0 0 0 4 AU1532, AU1419, AU1315, AU0640, AU0607, AU0506, AU0230 PRH1 edels 1 0 0 0 3 AU1791 PRH1 edups 1 0 0 0 2 AU0001 PRIC285 edups 3 0 1 0 5 AU1417, AU1210, AU0253, AU009 PRKAB2 gdups 2 0 3 0 3 AU1688, AU1610, AU1163 PRKAR1B gdups 1 0 0 0 2 AU0385 PRKG1 edels 2 0 0 0 3 AU0688, AU1619 PROP1 gdups 3 0 0 0 3 AU0718, AU1298, AU1231 PRPF18 edups 2 0 0 0 2 AU1699, AU0880 PRR4 edels 1 0 0 0 3 AU1791 PRR4 edups 1 0 0 0 2 AU0001 PRR5 edups 3 0 0 0 3 AU2005, AU1273, AU1055, AU1963, AU0481 PSCD2 gdups 4 0 0 0 5 AU0542, AU1610, AU1527, AU0795 PSG3 edels 1 0 0 1 2 AU1073 PSG8 edels 1 0 0 1 2 AU1073 PSKH1 gdups 4 0 0 0 5 AU0647, AU1368, AU1055, AU0305 PSMD8 edels 1 0 0 0 2 AU1685 PSMD8 gdups 2 0 0 0 3 AU1685, AU1273, AU0618, AU0379, AU0796 PTOV1 gdups 2 0 1 0 2 AU1273, AU1072, AU0880, AU0698, AU0520, AU0068 PTRH1 gdups 2 0 0 0 2 AU1174, AU1164, AU1650 PTTG1IP gdups 2 0 0 0 2 AU1227, AU1039, AU0753, AU0158 PWWP2 edups 1 0 0 0 2 AU1047, AU0786 QSER1 edels 1 0 0 3 2 AU0361 QSOX2 edups 2 0 1 0 3 AU1055, AU0247, AU0288 RAB11B gdups 2 0 0 0 2 AU1592, AU1209, AU1189, AU1174, AU0899, AU0806 RAB23 edels 1 0 0 0 2 AU1215, AU0455 RAB35 edups 3 0 0 0 3 AU0563, AU0411, AU0386 RAB39 gdups 2 0 0 1 3 AU0521, AU0352 RAB3A gdups 2 0 0 0 2 AU1277, AU1174, AU0947, AU0520, AU0991 RABGAP1L edels 2 0 0 12 3 AU1016, AU0616 RAFTLIN edels 1 0 0 1 2 AU0862 RAI1 edups 5 0 0 0 8 AU1713, AU1607, AU0993, AU0932, AU0922, AU0920, AU0585, AU0504, AU0483, AU0455, AU0289, AU0236, AU0186, AU0173 RALBP1 edels 1 0 0 0 2 AU1301 RANBP1 gdups 3 0 4 0 3 AU1174, AU0520, AU0018, AU0991, AU0049 RANBP10 gdups 3 0 0 0 4 AU0647, AU1368, AU1055 RANBP6 gdups 1 0 0 0 2 AU1699 RARG edups 1 0 0 0 2 AU0506 RAX2 gdups 3 0 0 0 3 AU0520, AU0991, AU0866, AU0806 RBMS3 edels 1 0 0 0 2 AU0254 RBMXL2 gdups 1 0 0 0 2 AU1309 RCD-8 gdups 4 0 0 0 5 AU1368, AU1055, AU0647, AU0305 RDH13 edels 1 0 0 0 2 AU1880 RNF111 edups 3 0 0 0 3 AU0763, AU1312, AU0039 RNF111 gdups 1 0 0 0 2 AU0467 RNF126 edups 1 0 0 0 2 AU1054 RNF133 edels 3 0 1 0 4 AU0733, AU0109, AU0029 RNF148 edels 3 0 1 0 4 AU0733, AU0109, AU0029 RNF44 edups 5 0 0 1 8 AU0629, AU0620, AU0034, AU0603, AU0563 ROCK1 edels 2 0 0 0 2 AU0190, AU0125 ROPN1B gdups 1 0 0 0 2 AU0911 RPL9 gdups 1 0 0 0 2 AU0158 RPS15 gdups 8 0 0 0 8 AU1778, AU1632, AU1368, AU1353, AU1277, AU1212, AU1207, AU1174, AU1164, AU1099, AU0974, AU0939, AU0934, AU0924, AU0899, AU0883, AU0795, AU0753, AU0081, AU1944, AU1527, AU1033, AU0866, AU0835 RPS19 edups 3 0 0 0 4 AU0712, AU0515, AU0025 RUVBL1 gdups 1 0 0 0 2 AU0835 RYR2 edups 3 0 0 2 3 AU1344, AU1285, AU1257 SACS gdups 2 0 0 1 2 AU1347, AU0965 SBF1 gdups 4 0 0 0 4 AU1764, AU1212, AU1174, AU1164, AU0974, AU0899, AU0616, AU1944, AU1216 SCP2 gdups 1 0 0 0 2 AU1811 SEC11L1 edels 1 0 0 0 3 AU0561 SEC61A1 gdups 1 0 0 0 2 AU0835 SEMA6B gdups 2 0 0 0 2 AU1164, AU1099, AU0947, AU0934, AU0616, AU0866 SEMA7A edups 2 0 0 0 2 AU1193, AU1055, AU0125 SETD4 gdups 2 0 0 0 3 AU1227, AU0753, AU0316, AU0158 SF3B3 gdups 1 0 0 0 2 AU1551, AU0686 SH2D3C gdups 2 0 0 0 2 AU1174, AU1164, AU0932, AU0298, AU1650 SH3TC1 edups 2 0 1 0 4 AU1650, AU1226, AU1137, AU0897, AU0773, AU0481 SH3YL1 edels 1 0 0 0 2 AU0385 SHB edups 2 0 0 0 2 AU1002, AU0640, AU0991, AU0796 SHD gdups 2 0 0 0 2 AU1164, AU1099, AU0947, AU0934, AU0991 SIAHBP1 gdups 2 0 0 1 2 AU0773, AU1944, AU0796 SIRT4 edups 2 0 0 0 4 AU1301, AU1194, AU0756 SKIV2L2 edels 6 0 0 1 6 AU1907, AU1823, AU1511, AU1616, AU1448, AU1407, AU1054, AU0242 SLC12A8 gdups 1 0 0 0 2 AU0911 SLC16A5 edups 3 0 0 0 7 AU1038, AU0307, AU0932 SLC17A3 edels 1 0 0 0 2 AU0208 SLC18A1 edels 2 0 0 0 4 AU1072, AU0043 SLC22A18 edups 3 0 1 0 3 AU1323, AU1072, AU0974, AU0816, AU0481 SLC24A3 edups 1 0 0 0 2 AU1321 SLC25A1 gdups 3 0 4 0 3 AU0018, AU0991, AU0049 SLC25A34 edels 3 0 0 2 3 AU1185, AU0932, AU1030, AU0319, AU0063 SLC26A11 gdups 3 0 0 0 3 AU2005, AU1277, AU1164, AU1072, AU0947 SLC27A5 gdups 2 0 0 0 2 AU1164, AU0934, AU0816, AU0786 SLC28A1 edups 2 0 0 0 3 AU0827, AU0109, AU0056 SLC2A4RG gdups 3 0 0 0 3 AU1912, AU1368, AU1277, AU1207, AU0947, AU0939, AU0934, AU0922, AU0543, AU0520, AU0109 SLC2A6 gdups 2 0 0 0 2 AU1273, AU0897, AU0520, AU1650, AU0806 SLC35A2 gdups 1 0 0 0 2 AU1465 SLC41A3 gdups 1 0 0 0 2 AU0911 SLC43A2 edups 1 0 0 0 3 AU0034 SLC45A1 edups 2 0 0 0 3 AU1486, AU1416, AU0253 SLC5A10 edups 2 0 0 1 2 AU1197, AU0665 SLC5A8 gdups 1 0 0 0 2 AU1317 SLC6A15 edels 3 0 0 1 4 AU1482, AU0993, AU0599, AU0180, AU0043, AU0800 SLC6A7 edels 1 0 0 0 2 AU1171 SLC7A10 gdups 3 0 0 0 3 AU0816, AU1033, AU0991, AU0806 SLC7A9 edups 1 0 0 0 2 AU1289 SLC9A5 gdups 12 0 0 0 16 AU0939, AU0899, AU0722, AU0610, AU0450, AU0210, AU0028, AU1368, AU0991, AU0835 SLCO1A2 edels 3 0 0 12 3 AU1368, AU1098, AU0753, AU0681, AU0653, AU0134 SLCO1B3 edups 2 0 0 0 3 AU1953, AU1916 SMARCA4 edups 2 0 0 0 3 AU1289, AU1190 SMU1 edels 1 0 0 0 2 AU1544 SMU1 edups 1 0 0 0 2 AU0822 SNRPB2 gdups 2 0 1 0 2 AU1158, AU1143 SNRPN gdups 5 0 8 0 8 AU1331, AU0106, AU0065, AU1135, AU0233 SNURF gdups 5 0 8 0 8 AU1331, AU0106, AU0065, AU1135, AU0233 SNW1 gdups 1 0 0 0 2 AU0755 SNX14 edels 2 0 0 5 2 AU0780, AU0622, AU1048, AU0139 SNX25 edups 2 0 0 0 3 AU1730, AU1143, AU1010 SNX4 gdups 1 0 0 0 2 AU0911 SNX5 gdups 1 0 0 0 2 AU1520, AU0752 SNX9 edups 1 0 0 0 2 AU1227 SOX3 edels 1 0 0 0 2 AU1823 SPACA5B gdups 3 0 0 0 3 AU1083, AU0133, AU0034 SPANXB1 edels 1 0 0 0 2 AU1823 SPANXB2 edels 1 0 0 0 2 AU1823 SPATA21 edups 1 0 0 0 2 AU1344, AU0081 SPG7 gdups 1 0 0 0 2 AU0907 SPON2 edels 5 0 0 2 6 AU1318, AU1231, AU1185, AU1085, AU1083, AU0782 SPRED3 edels 1 0 0 0 2 AU1685 SPRED3 gdups 4 0 0 0 5 AU1273, AU0680, AU0618, AU0379, AU0325, AU0001, AU0796 SPRN gdups 2 0 0 1 3 AU1482, AU1342, AU0653, AU1165 SRL edups 3 0 0 0 3 AU1193, AU0767, AU1762, AU0633, AU0066 SSSCA1 edels 3 0 1 0 4 AU1520, AU1439, AU1102 SSU72 edups 2 0 0 0 2 AU1010, AU0275, AU0268 SSX5 gdups 3 0 0 0 3 AU1083, AU0133, AU0034 SSX6 gdups 2 0 0 0 2 AU0034, AU0133 ST3GAL2 gdups 1 0 0 0 2 AU1551, AU1445, AU0686 STAM2 edups 1 0 0 0 3 AU1525, AU1454, AU0958 STEAP3 edups 2 0 0 1 3 AU1622, AU1444, AU1684 STIP1 gdups 5 0 0 0 5 AU1207, AU0947, AU0934, AU1164, AU1033, AU0866, AU0835, AU0806 SUCLG2 edels 2 0 1 0 3 AU0034, AU0122 SULT2A1 edels 2 0 0 1 2 AU1424, AU1222, AU1373 SUPT4H1 gdups 2 0 0 0 2 AU1189, AU0991, AU0806 SYNGR2 gdups 3 0 0 0 3 AU1174, AU0947, AU0991, AU0835, AU0806 SYT9 gdups 1 0 0 0 2 AU1309 TAF11 gdups 2 0 0 1 2 AU1575, AU1412, AU0668 TANC1 edels 2 0 0 0 2 AU1334, AU0378, AU0381 TAS2R44 edels 1 0 0 0 3 AU1791 TAS2R44 gdups 1 0 0 0 2 AU0001 TAS2R48 edels 1 0 0 0 3 AU1791 TAS2R49 edels 1 0 0 1 3 AU1791 TBC1D4 edels 1 0 0 0 2 AU1565 TCERG1 edels 2 0 0 0 2 AU0808, AU0679, AU0453 TCP10L gdups 3 0 0 0 3 AU1227, AU0753, AU0180, AU0910, AU0158 TDP1 edups 2 0 0 0 2 AU1579, AU0980, AU0923, AU0314, AU1313 TEKT3 edels 1 0 0 1 2 AU0149 TEKT3 gdups 1 0 0 0 2 AU0707 TESK2 edels 1 0 0 1 2 AU0029 TF edups 2 0 0 0 2 AU0771, AU0752 TH edels 2 0 0 0 2 AU1231, AU1102, AU1098 THAP11 gdups 3 0 0 0 4 AU0647, AU1368, AU1055 TIGD1 gdups 1 0 0 0 2 AU1213 TIMM17B gdups 1 0 0 0 2 AU1465 TJP3 gdups 5 0 0 0 5 AU1411, AU1072, AU0520, AU1944, AU0991, AU0866, AU0806 TK1 gdups 2 0 0 0 2 AU1174, AU0947, AU0991, AU0835 TLL1 edups 1 0 0 0 2 AU1379, AU1352, AU1234 TLN2 edels 1 0 0 0 2 AU1261 TMC7 gdups 1 0 0 0 2 AU0993 TMCO3 edels 1 0 0 0 2 AU1327 TMCO7 edups 2 0 0 0 2 AU1353, AU1220, AU0312 TMEM104 edups 1 0 0 0 2 AU0254 TMEM112 gdups 3 0 0 0 3 AU1348, AU1174, AU0947, AU0932, AU0678, AU0520, AU1216, AU1159, AU0796 TMEM138 gdups 2 0 0 0 3 AU1323, AU0918, AU0246 TMEM146 edels 1 0 0 0 2 AU1135 TMEM16E edels 2 0 0 0 2 AU0604, AU0180 TMEM18 edels 1 0 0 0 2 AU0385 TMEM56 edels 1 0 0 0 2 AU0028 TNFAIP8L1 gdups 2 0 0 0 2 AU1164, AU1099, AU0947, AU0934, AU0616 TNFRSF10D edups 1 0 0 1 2 AU0745, AU0267 TNFRSF12A edels 2 0 1 0 2 AU1085, AU1338, AU1107 TNFRSF14 gdups 4 0 0 0 4 AU0934, AU0899, AU0880, AU0841, AU0816, AU0693, AU0520, AU0161, AU1409, AU0866 TNFRSF19 gdups 2 0 0 1 2 AU1347, AU0965 TNFRSF21 edups 1 0 0 0 3 AU0379 TNFRSF25 edels 1 0 0 8 2 AU1301 TNFRSF8 edups 3 0 0 0 5 AU1344, AU1244, AU0241 TNIP2 gdups 2 0 1 0 2 AU1338, AU0947, AU0866 TNNT1 edels 1 0 0 0 2 AU1301 TNS3 edups 1 0 0 0 2 AU0780 TOR2A gdups 2 0 0 0 2 AU1174, AU1164, AU1650 TP73 edels 2 0 0 1 2 AU1171, AU1157, AU1098, AU0809, AU0614, AU1231 TPPP edels 8 0 0 1 9 AU1867, AU1243, AU1235, AU1231, AU1213, AU1185, AU1157, AU0951, AU0802, AU1373, AU1333, AU1105 TPPP gdups 1 0 0 0 2 AU1172, AU0934 TRADD gdups 1 0 0 0 2 AU0962, AU0210 TRAPPC5 gdups 1 0 0 0 2 AU1730 TRDN edups 1 0 0 0 2 AU0977 TRHDE edels 2 0 0 0 2 AU1215, AU0752, AU0736, AU0668, AU0465, AU0972 TRIM58 edels 2 0 0 0 2 AU1368, AU0951 TRPM1 gdups 2 0 0 1 3 AU1208, AU0520 TRPM5 edels 1 0 0 0 2 AU1612 TRPS1 edels 1 0 0 0 2 AU0063 TRPT1 gdups 5 0 0 0 5 AU1207, AU0947, AU0934, AU1164, AU1033, AU0866, AU0835, AU0806 TSC2 edups 2 0 0 0 3 AU0482, AU0056 TSNAXIP1 gdups 3 0 0 0 4 AU0647, AU1368, AU1055 TSPAN32 edels 1 0 0 0 2 AU1921, AU1798 TSSK2 gdups 3 0 4 0 3 AU0018, AU0991, AU0049 TTC16 gdups 2 0 0 0 2 AU1174, AU1164, AU1650 TTC9B gdups 1 0 0 0 2 AU1054 TTYH3 edels 2 0 0 11 2 AU1437, AU1285, AU0782 TUSC3 edels 2 0 0 0 2 AU0241, AU0827 TUSC5 gdups 1 0 0 1 2 AU1575 TXNRD2 gdups 3 0 4 0 3 AU0018, AU0991, AU0049 UBE1L2 edups 1 0 0 0 2 AU1688 UBE2O edups 4 0 0 0 7 AU0736, AU0696, AU0325, AU0289, AU0215 UBE3A gdups 5 0 8 0 8 AU1331, AU0106, AU0065, AU1135, AU0233 UBR1 edups 2 0 0 1 3 AU1644, AU0809, AU1254 UBXD1 gdups 2 0 0 0 2 AU1273, AU1174, AU1099, AU1072, AU1944, AU1216 UFD1L gdups 3 0 4 0 3 AU0018, AU0991, AU0049 UFM1 gdups 1 0 0 0 2 AU1403 UGCGL2 edels 1 0 0 0 2 AU0700, AU0696 UGDH gdups 1 0 0 0 2 AU0158 UGT1A5 edels 2 0 0 0 3 AU1535, AU1458, AU1277, AU1059, AU1535, AU1059 UNC13C edels 1 0 0 1 2 AU1589, AU0729 UNC84A gdups 1 0 0 0 2 AU0385 UNC93B1 edels 3 0 1 0 3 AU1553, AU0803, AU0746 UNCX4.1 gdups 3 0 0 0 4 AU1632, AU1348, AU1174, AU0922, AU0899, AU0385, AU0340, AU1527 UNQ2446 gdups 4 0 0 0 5 AU0647, AU1368, AU1055, AU0305 URP2 gdups 5 0 0 0 5 AU1207, AU0947, AU0934, AU1164, AU1033, AU0866, AU0835, AU0806 USF2 edels 1 0 0 0 2 AU1553, AU1301 USH1G gdups 2 0 0 0 2 AU0298, AU0806 USH2A edels 3 0 0 0 4 AU0920, AU0622, AU0352, AU0137 USP20 edups 2 0 0 0 2 AU0076, AU0008 UTRN edups 2 0 0 0 3 AU1496, AU1524 VAC14 gdups 1 0 0 0 2 AU1551 VANGL1 gdups 1 0 0 0 2 AU0651 VCX2 gdups 3 0 0 0 5 AU0661, AU0268, AU0165, AU1798 VCX3A gdups 2 0 0 0 2 AU0943, AU0842, AU0708, AU0264 VDP edels 1 0 0 0 2 AU0915 VIPR2 edups 2 0 0 0 2 AU0159, AU1283 VPS37B gdups 4 0 0 0 6 AU1378, AU1289, AU0899, AU0836, AU0688, AU0001, AU0382 VPS4A edups 1 0 0 0 3 AU0733 WASF3 edups 5 0 0 1 8 AU1565, AU1054, AU1000, AU0610, AU0509, AU0138, AU0362 WDR18 edels 2 0 0 9 2 AU1231, AU0809, AU1171 WDR71 edups 2 0 0 0 2 AU0997, AU0290 WDR73 edels 1 0 0 0 3 AU0561 WDR78 edups 3 0 0 0 7 AU1916, AU1880, AU1791, AU1368 WNT7A edups 3 0 0 0 4 AU0633, AU0121, AU0068 WWP2 edups 1 0 0 0 2 AU0718 XG edels 2 0 0 0 4 AU1059, AU0338 XYLT1 edels 1 0 0 0 2 AU0791 YTHDF1 edels 1 0 0 0 2 AU0746 ZBTB20 edels 1 0 0 0 2 AU1055 ZC3H7B edups 5 0 0 0 7 AU1582, AU1226, AU1158, AU1030, AU0947, AU0346, AU0017, AU1359 ZCCHC14 edups 1 0 0 0 2 AU0771, AU0575 ZDHHC1 gdups 3 0 0 0 3 AU1207, AU0962, AU1368, AU0991, AU0835 ZDHHC11 edels 2 0 0 0 2 AU1185, AU1056, AU0951, AU1105 ZFAND2A gdups 1 0 0 1 2 AU1174, AU0922, AU0385 ZFP37 edels 1 0 0 1 2 AU1247 ZFPM2 edels 1 0 0 0 2 AU0725, AU0452, AU0259 ZIC3 edels 1 0 0 0 2 AU1823 ZMYND19 gdups 2 0 0 0 2 AU0767, AU0622 ZNF135 edels 1 0 0 0 2 AU0179 ZNF141 edels 2 0 0 0 2 AU1251, AU1251, AU0032 ZNF148 gdups 1 0 0 0 2 AU0911 ZNF208 edels 1 0 0 0 2 AU0145 ZNF208 gdups 2 0 0 2 3 AU1338, AU1292 ZNF214 gdups 1 0 0 0 2 AU1309 ZNF215 gdups 1 0 0 0 2 AU1309 ZNF257 edels 2 0 0 1 3 AU1277, AU0145 ZNF324 gdups 2 0 0 0 2 AU1174, AU0934, AU0816, AU1527, AU0481 ZNF37A gdups 2 0 0 0 3 AU0257, AU1403 ZNF446 gdups 2 0 0 0 2 AU1174, AU0934, AU0816, AU1527, AU0481 ZNF451 edels 1 0 1 0 2 AU1215 ZNF467 edups 2 0 0 0 2 AU0412, AU1048 ZNF492 edels 1 0 0 0 2 AU0145 ZNF499 gdups 2 0 0 0 2 AU1164, AU0934, AU0816, AU0786 ZNF574 edels 2 0 0 5 2 AU1305, AU1286 ZNF592 edels 1 0 0 0 3 AU0561 ZNF650 edels 2 0 0 2 2 AU0767, AU0419, AU0264 ZNF676 edels 2 0 0 0 3 AU1277, AU0145 ZNF74 gdups 3 0 3 1 3 AU1334, AU0049, AU0018 ZNF85 edels 2 0 0 1 2 AU0911, AU0809, AU0677, AU0201, AU0980 ZNF99 edels 1 0 0 0 2 AU0145 ZSCAN2 edels 1 0 0 0 3 AU0561

TABLE 2 Description of AGRE sample used in the analysis. CHOP Control Cohort: 1110 samples genotyped 1070 retained after QC (96% pass rate) NINDS Control Cohort: 540 samples genotyped 418 retained after QC (77% pass rate) AGRE Family Cohort: 4163 samples genotyped on v3 arrays 3832 retained after QC (92% pass rate) ACC Cases & Controls: see Glessner et al., 2009, Nature for a full description

TABLE 3 Summary of CNVs in AGRE cases, first-degree relatives, and unrelated controls. AGRE unaffected NINDS CHOP AGRE affected (siblings/parents) controls controls N= 1673 2159 418 1070 Mean # CNV 24.7 25.2 20.5 23.3 Mean # eDels 2.0 2.1 2.3 2.6 Mean # eDups 6.0 6.3 2.2 4.2 Mean # gDups 4.0 4.1 1.0 2.5

TABLE 4 Shared by Region # SNP Length (bp) Type AGRE ID Scored status Inheritance status affected sibling? Previous reports 15q11-13 1246 5,902,313 dup AU010601 parent [22] 15q11-13 1246 5,902,313 dup AU010604 Autism inherited No [22] 15q11-13 1246 5,902,313 dup AU1331202 parent 15q11-13 1246 5,902,313 dup AU1331302 Autism inherited Yes 15q11-13 1246 5,902,313 dup AU1331303 Autism inherited Yes 15q11-13 1130 5,008,629 dup AU006501 parent 15q11-13 1130 5,008,629 dup AU006503 Spectrum inherited Yes AGRE cytogenetic annotation 15q11-13 1130 5,008,629 dup AU006504 Autism inherited Yes AGRE cytogenetic annotation, [21] 15q11-13 1130 5,008,629 dup AU1135202 Autism de novo NA 15q11-13 1127 4,993,869 dup AU023303 Spectrum NA Yes [22] 15q11-13 1127 4,993,869 dup AU023304 Autism NA Yes [21, 22] 15q11-13 1127 4,993,869 dup AU1607307 Autism de novo No 15q11-13 569 3,540,078 del AU1024202 parent 15q11-13 569 3,540,078 del AU1024301 Autism inherited NA 15q11-13 437 1,347,744 dup AU038504 Autism de novo No [22] 15q11-13 287 1,578,642 dup AU1208301 Autism de novo No 15q11-13 273 1,517,841 dup AU1875202 parent 15q11-13 98 572,462 dup AU052003 Autism NA Yes [21] 15q11-13 96 572,462 dup AU052004 Autism NA Yes 16p11.2 47 530,466 del AU0154302 Autism de novo Yes [10, 11] 16p11.2 47 530,466 del AU0154303 Autism de novo Yes [10, 11, 21] 16p11.2 47 530,466 del AU029803 Autism de novo No [10, 11, 21] 16p11.2 47 530,466 del AU041905 Autism de novo No [10, 11, 21] 16p11.2 47 530,466 del AU0938301 Autism de novo No [10, 11, 21] 16p11.2 47 530,466 dup AU002901 parent [11] 16p11.2 47 530,466 dup AU002903 Autism inherited Yes [11] 16p11.2 47 530,466 dup AU002904 None inherited [11] 16p11.2 47 530,466 dup AU002905 Autism inherited Yes [10, 11] 22q11.21 512 2,534,567 dup AU001802 parent [22] 222q11.21 512 2,534,567 dup AU001804 Autism inherited No [21, 22] 22q11.21 512 2,534,567 dup AU004903 Autism de novo No [21, 22] 22q11.21 335 1,429,207 dup AU0991301 Autism NA No 22q11.21 177 728,859 dup AU1334201 parent 22q11.21 177 728,859 dup AU1334302 Spectrum inherited No 22q11.21 149 601,423 del AU1555302 Autism NA NA doc10.1371/journal.pgen.1000536.1001

TABLE 5 TaqMan primers and probes used in CNV validation. Reporter and reporter quencher are FAM and  NFQ, respectively, unless noted AssaBSA15 Target = human BCL9 forward primer = CTGAGTTGATTTTTGGTTAAGTTGATTCCTT reverse primer = GGACCTGAAATTCGAGGATTCTGT reporter sequence = TAGGAATGGGCATTAATAC AssaBSA16 Target = human NLRP3 forward primer = AGTGCAACCCAGGCTTTCTATTT reverse primer = GTGTTTCTAACGCACTTTTTGTCTCA reporter sequence = CAGACAACCTGTAAAAGC AssaBSA20 Target = human NKX3-2 forward primer = TGGAAGCTCTATTCGCTGTATTTTTTCT reverse primer = CCAAAAGTCGGGAAAAGACAGTTT reporter sequence = CATGCCCTCCTGGACGC AssaBSA21 Target = human HHIP-itg forward primer = TCATCTCAGTTGTGATCGTTCTGTTTT reverse primer = AGGGTGTGCAGAAATGGTACTTAATT reporter sequence = TCTACATCGTGAAATTAC AssaBSA22 Target = human 4q32.1 forward primer = TGAGTAACAGCATTTATCATGGCTTGA reverse primer = GGAAAAGGTTTTGAAAACATTGTTATCACAGT reporter sequence = CCTAAGATCAGGCAATTAG AssaBSA23 Target = human 6q16.1 forward primer = AGTGACAGTACATGCAACAGTTCAT reverse primer = GCTCCTCTGTAGCTGTCAGTTC reporter sequence = CTGTGCCAAACTTCA AssaBSA25 Target = human 8q21.2 forward primer = AGTGTAGGTGCAATCAAAGAGAATGA reverse primer = CTCAATTGTTTTAAAATATTGGGCAAAGTTCA reporter sequence = ATAAGTGGTTTAGCATTTCTG AssaBSA26 Target = human HPSE2-in forward primer = TCAGTGAGGTCTGGGTTCAATATCT reverse primer = TGCTGCTCATATGTTATCAAAGCATTATATCA reporter sequence = TTGGCTGTCCGCCTTGT AssaBSA27 Target = human TAT forward primer = GCTTCTTGGAGGCTGCTTTCT reverse primer = CACCACTGCCTGATCAGCTT reporter sequence = TTGGAAGGTAAAAATCTC AssaBSA28 Target = human PPP1R16B forward primer = CCAGCTGGTAATGTTGTCCTTCT reverse primer = GAGAGTAGCACGGGCTTCT reporter sequence = CACTCGCAGAACCCCA AssaBSA29 Target = human BHLHB4 forward primer = GCGTAGCCGTGGCTTAGT reverse primer = CCATGGCCGAGCTCAAGT reporter sequence = CAGGTACGCGTCCCC AssaBSA30 Target = human DMD forward primer = GATGGACTTCTTATCTGGATAGGTGGTA reverse primer = GAGTCTCAAATATAGAAACCAAAAATTGATGTGT reporter sequence = CAACATCTGTAAGCACATTAA AssaBSA32 Target = RNaseP endogenous control reporter = VIC; quencher = TAMRA; primer limited Part Number 4316844 (applied biosystems)

TABLE 6 gene class locus AGRE.Cases.Unrelated Map.Position.March.2006. Chr.Band ACRD? Combined.P ABCB9 gdups 120 3 chr12: 121979494-122025705 12q24.31 Yes 0.07 ABCC1 edups 144 3 chr16: 15950935-16144432 16p13.11 No 0.07 ACP6 gdups 15 3 chr1: 145585794-145608988 1q21.1 Yes 4.79E−03 ADAMTS5 gdups 198 2 chr21: 27212112-27260703 21q21.3 No 0.17 ADAMTSL1 edups 76 2 chr9: 18464098-18900948 9p22.2 No 0.17 ADCY1 edups 66 3 chr7: 45580646-45729237 7p13 No 0.07 ADM2 gdups 208 4 chr22: 49266878-49271732 22q13.33 Yes 0.03 AHR gdups 65 2 chr7: 17304832-17352294 7p21.1 Yes 0.37 APBA3 gdups 173 3 chr19: 3701771-3712673 19p13.3 No 0.07 APLP1 gdups 185 3 chr19: 41051241-41062539 19q13.12 Yes 0.07 ARHGEF16 edups 2 3 chr1: 3361100-3387537 1p36.32 No 0.07 ARID3A edups 168 4 chr19: 877037-923781 19p13.3 Yes 0.03 ARL11 gdups 123 4 chr13: 49100436-49106009 13q14.3 No 0.03 ARSA gdups 208 4 chr22: 49410316-49413473 22q13.33 Yes 0.10 ARSD edels 209 2 chrX: 2832011-2857392 Xp22.33 Yes 0.17 ARSD gdups 209 2 chrX: 2832011-2857392 Xp22.33 Yes 0.17 ARVCF gdups 203 4 chr22: 18337421-18384309 22q11.21 Yes 8.05E−04 ASCC3 edups 55 3 chr6: 101062791-101435961 6q16.3 No 0.07 ATCAY gdups 173 3 chr19: 3831639-3873184 19p13.3 No 0.07 ATP10A gdups 132 6 chr15: 23474952-23661412 15q12 Yes 9.28E−06 ATP6V0D1 gdups 149 3 chr16: 66029418-66072590 16q22.1 No 0.07 BC002942 gdups 208 5 chr22: 49288250-49292975 22q13.33 Yes 0.01 BCL9 gdups 15 3 chr1: 145479806-145564641 1q21.1 Yes 4.79E−03 BTBD4 edups 197 3 chr20: 61846322-61907300 20q13.33 Yes 0.07 BTN2A1 edels 53 2 chr6: 26566168-26577844 6p22.1 No 0.37 BXDC1 edups 56 2 chr6: 111409984-111453486 6q21 Yes 0.17 BZRAP1 edels 158 6 chr17: 53733597-53760477 17q22 No 8.05E−04 BZRAP1 edups 158 4 chr17: 53733597-53760477 17q22 No 0.03 C10orf72 edups 83 9 chr10: 49896258-49993560 10q11.22 Yes 2.08E−03 C11orf72 gdups 102 3 chr11: 67126927-67130753 11q13.2 No 0.07 C12orf38 gdups 121 2 chr12: 122721644-122758901 12q24 Yes 0.17 C15orf2 gdups 132 6 chr15: 22471634-22479686 15q11.2 Yes 3.79E−06 C19orf19 edels 167 3 chr19: 414347-425983 19p13.3 No 1.35E−04 C1orf93 gdups 1 4 chr1: 2508097-2512762 1p36.32 Yes 0.03 C1QTNF1 edels 163 8 chr17: 74531846-74557465 17q25.3 No 0.17 C21orf51 gdups 201 3 chr21: 34669619-34683322 21q22.11 No 0.34 C22orf25 gdups 203 3 chr22: 18384537-18433449 22q11.21 Yes 1.96E−03 C22orf29 gdups 203 3 chr22: 18213661-18222419 22q11.21 Yes 1.96E−03 C9orf28 edups 78 2 chr9: 128128949-128309140 9q33.3 No 0.17 CA5A edups 152 3 chr16: 86479126-86527613 16q24.2 Yes 0.07 CA6 edels 6 3 chr1: 8928509-8957733 1p36.23 No 0.03 CACHD1 edups 13 3 chr1: 64709063-64931329 1p31.3 No 0.07 CACNA2D4 edups 108 5 chr12: 1771384-1898131 12p13.33 Yes 0.01 CAND2 edels 34 2 chr3: 12813171-12851301 3p25.1 No 0.17 CARD11 edups 60 3 chr7: 2912295-3050105 7p22.2 No 0.19 CARD9 gdups 81 5 chr9: 138378229-138387954 9q34.3 Yes 4.79E−03 CBLN3 gdups 127 4 chr14: 23965582-23968571 14q12 No 0.03 CBR1 gdups 202 2 chr21: 36364155-36367332 21q22.12 Yes 0.17 CCL13 gdups 157 2 chr17: 29707584-29709741 17q12 Yes 0.68 CD8A gdups 26 2 chr2: 86865240-86889030 2p11.2 No 0.07 CDC45L gdups 203 3 chr22: 17846982-17888135 22q11.21 Yes 1.96E−03 CDH17 edels 73 2 chr8: 95208566-95289986 8q22.1 No 0.17 CEBPA gdups 184 3 chr19: 38482543-38485460 19q13.11 Yes 0.19 CELSR1 edups 207 6 chr22: 45134397-45311731 22q13.31 Yes 4.79E−03 CENPT gdups 150 3 chr16: 66419565-66425300 16q22.1 No 0.07 CERK edups 207 3 chr22: 45458984-45512833 22q13.31 Yes 0.07 CERK gdups 207 5 chr22: 45458984-45512833 22q13.31 Yes 0.01 CGB1 gdups 191 2 chr19: 54230638-54231885 19q13.33 No 0.54 CGB2 gdups 191 2 chr19: 54226942-54228307 19q13.33 No 0.54 CGB5 gdups 191 2 chr19: 54238875-54240378 19q13.33 No 0.54 CGB8 gdups 191 2 chr19: 54242709-54244212 19q13.33 No 0.54 CGI-38 gdups 149 3 chr16: 65981213-65984922 16q22.1 No 0.07 CHD1L gdups 15 2 chr1: 145180915-145234065 1q21.1 Yes 0.01 CHD9 edups 146 2 chr16: 51646446-51918914 16q12.2 No 0.07 CLCNKA edels 9 4 chr1: 16220953-16233132 1p36.13 No 0.03 CLDN17 gdups 199 2 chr21: 30459753-30460945 21q21.3 No 0.17 CLDN5 gdups 203 3 chr22: 17890547-17895068 22q11.21 Yes 1.96E−03 CLDN8 gdups 199 2 chr21: 30508195-30510262 21q22.11 No 0.17 CLTCL1 gdups 203 3 chr22: 17546989-17659239 22q11.21 Yes 1.96E−03 COL16A1 edups 11 5 chr1: 31890435-31942507 1p35.2 No 0.05 COL27A1 edels 77 2 chr9: 115957661-116114612 9q32 Yes 0.37 COMT gdups 203 3 chr22: 18309256-18336539 22q11.21 Yes 1.96E−03 CORO7 gdups 143 4 chr16: 4344546-4406572 16p13.3 No 0.03 COX4I1 gdups 151 3 chr16: 84390697-84398109 16q24.1 No 0.07 CPNE7 edups 153 3 chr16: 88169677-88191155 16q24.3 No 0.07 CREB3L3 gdups 173 9 chr19: 4104629-4124050 19p13.3 No 3.30E−04 CRELD2 gdups 208 3 chr22: 48698287-48707192 22q13.33 Yes 0.07 CSTF2T gdups 86 2 chr10: 53125253-53129357 10q11.23 Yes 0.17 CYBASC3 gdups 98 2 chr11: 60872856-60886305 11q12.2 No 0.17 CYP4A22 gdups 12 2 chr1: 47375694-47388000 1p33 No 0.17 CYP4F22 edels 178 3 chr19: 15497144-15524127 19p13.12 No 0.34 CYP4X1 gdups 12 2 chr1: 47261827-47289009 1p33 No 0.17 CYP4Z1 gdups 12 2 chr1: 47305634-47356577 1p33 No 0.17 DACH1 edels 126 8 chr13: 70910099-71339331 13q21.33 No 0.24 DAK gdups 98 4 chr11: 60857230-60872806 11q12.2 No 0.03 DAPK3 gdups 173 7 chr19: 3909452-3920826 19p13.3 No 1.96E−03 DAZAP1 gdups 169 8 chr19: 1358584-1386683 19p13.3 Yes 8.05E−04 DBH edups 79 2 chr9: 135491306-135514287 9q34.2 Yes 0.17 DDB1 gdups 98 3 chr11: 60823510-60857143 11q12.2 No 0.07 DGCR14 gdups 203 3 chr22: 17497793-17512190 22q11.21 Yes 1.96E−03 DGCR2 gdups 203 3 chr22: 17403795-17489967 22q11.21 Yes 1.96E−03 DGCR8 gdups 203 3 chr22: 18447814-18479395 22q11.21 Yes 1.96E−03 DGKB edels 64 8 chr7: 14151199-14909359 7p21.2 Yes 8.05E−04 DHX29 edels 46 3 chr5: 54587831-54639278 5q11.2 No 0.19 DIDO1 gdups 194 4 chr20: 60979535-61039719 20q13.33 Yes 0.03 DKFZP686A10121 edels 67 2 chr7: 89813926-89854586 7q21.13 No 0.68 DLGAP1 edels 165 4 chr18: 3486030-3870135 18p11.31 No 0.03 DNAJC17 edups 134 7 chr15: 38847363-38886954 15q15.1 No 1.96E−03 DOCK6 gdups 177 4 chr19: 11170973-11234157 19p13.2 No 0.03 DPP10 edels 28 2 chr2: 114916346-116319798 2q14.1 Yes 0.17 DSCR1 gdups 201 3 chr21: 34810654-34908615 21q22.12 No 0.34 DUSP13 edups 87 2 chr10: 76524196-76538976 10q22.2 No 0.17 E2F4 gdups 148 12 chr16: 65783569-65790322 16q22.1 No 2.27E−05 EDG5 gdups 174 3 chr19: 10195520-10196581 19p13.2 No 0.07 EEF2 gdups 173 7 chr19: 3927055-3936461 19p13.3 No 1.96E−03 EFHA2 edels 69 2 chr8: 16929119-17024516 8p22 No 0.17 ELMO3 gdups 148 12 chr16: 65790515-65795433 16q22.1 No 2.27E−05 ELP4 edels 95 2 chr11: 31487873-31761903 11p13 No 0.94 EPRS edels 18 2 chr1: 218208567-218286623 1q41 No 0.17 ERGIC1 edups 49 4 chr5: 172193928-172312287 5q35.1 No 0.03 FAM89B edels 101 3 chr11: 65096396-65098245 11q13.1 No 0.03 FHOD1 gdups 148 13 chr16: 65820795-65838926 16q22.1 No 9.28E−06 FKSG24 gdups 180 3 chr19: 18165040-18168550 19p13.11 No 0.07 FLJ10379 gdups 23 2 chr2: 45469324-45691937 2p21 Yes 0.54 FLJ12529 edups 99 6 chr11: 60926697-60953959 11q12.2 No 4.79E−03 FLJ12949 edups 175 9 chr19: 10525267-10536683 19p13.2 No 3.30E−04 FLJ14668 gdups 25 3 chr2: 70376612-70382724 2p14 Yes 0.07 FLJ21865 edels 163 3 chr17: 74582614-74596276 17q25.3 No 0.93 FLJ38991 gdups 42 3 chr4: 74140668-74154286 4q13.3 Yes 0.07 FLJ41603 edups 48 3 chr5: 148941328-148994720 5q33.1 No 0.07 FLJ41993 gdups 208 3 chr22: 48775069-48793182 22q13.33 Yes 0.07 FLJ43860 edups 74 3 chr8: 142513111-142586512 8q24.3 No 0.07 FLJ44894 edels 181 2 chr19: 20366360-20399602 19p12 No 0.94 FLRT1 gdups 100 6 chr11: 63627938-63643221 11q13.1 No 4.79E−03 FLYWCH1 edels 141 3 chr16: 2901981-2941209 16p13.3 No 4.79E−03 FMO5 gdups 15 2 chr1: 145124462-145163569 1q21.1 Yes 0.01 FUT10 edups 71 3 chr8: 33347884-33450206 8p12 No 0.07 GABRA5 gdups 132 5 chr15: 24663151-24777095 15q12 Yes 2.27E−05 GABRB3 gdups 132 6 chr15: 24339786-24767329 15q12 Yes 3.79E−06 GABRG3 gdups 132 5 chr15: 24799263-25451622 15q12 Yes 5.54E−05 GALNT13 edels 31 4 chr2: 154436672-155018734 2q23.3 Yes 0.01 GAMT gdups 169 8 chr19: 1348089-1352552 19p13.3 Yes 8.05E−04 GEMIN4 edups 154 2 chr17: 594411-602251 17p13.3 No 0.17 GGN gdups 186 4 chr19: 43566745-43570508 19q13.2 No 0.03 GJA8 gdups 15 3 chr1: 145841560-145848017 1q21.1 Yes 0.03 GMPS edels 38 3 chr3: 157071019-157138215 3q25.31 No 0.07 GNA11 gdups 171 6 chr19: 3045408-3072452 19p13.3 Yes 4.79E−03 GNB1L gdups 203 3 chr22: 18150747-18222462 22q11.21 Yes 1.96E−03 GNG7 edups 170 2 chr19: 2465451-2506186 19p13.3 No 0.07 GOLGA8E gdups 130 2 chr15: 20986537-20999858 15q11.2 Yes 0.17 GPR146 gdups 62 2 chr7: 1061447-1065423 7p22.3 Yes 0.37 GPR89A gdups 15 3 chr1: 144475774-144538430 1q21.1 No 0.03 GRIK5 edels 188 3 chr19: 47194317-47261797 19q13.2 No 0.71 GSCL gdups 203 3 chr22: 17516504-17517796 22q11.21 Yes 1.96E−03 GYG2 edels 209 2 chrX: 2756859-2810858 Xp22.33 Yes 0.17 GYG2 gdups 209 2 chrX: 2756859-2810858 Xp22.33 Yes 0.17 HES7 gdups 155 11 chr17: 7965024-7968127 17p13.1 No 5.54E−05 HIRA gdups 203 3 chr22: 17698224-17799219 22q11.21 Yes 1.96E−03 HNF4G edels 72 2 chr8: 76482732-76641600 8q21.11 No 0.17 HPCAL1 edups 22 4 chr2: 10360491-10485193 2p25.1 No 0.01 HSD11B2 gdups 149 3 chr16: 66022537-66028953 16q22.1 No 0.07 HSPC171 gdups 148 13 chr16: 65818517-65820683 16q22.1 No 9.28E−06 HTF9C gdups 203 3 chr22: 18479398-18484768 22q11.21 Yes 1.96E−03 IFI30 gdups 180 4 chr19: 18145579-18149927 19p13.11 No 0.03 INHBB gdups 30 3 chr2: 120820189-120825853 2q14.2 No 0.07 ITGB1BP3 gdups 173 7 chr19: 3884101-3893412 19p13.3 No 1.96E−03 KCNAB2 edups 3 5 chr1: 5974113-6083840 1p36.31 No 4.79E−03 KCNE1 gdups 201 3 chr21: 34740858-34806443 21q22.12 No 0.34 KCNE2 gdups 201 3 chr21: 34658193-34665307 21q22.11 No 0.34 KCNH7 edups 32 2 chr2: 162936163-163403274 2q24.2 No 0.17 KCNJ14 gdups 190 3 chr19: 53650578-53661179 19q13.32 No 0.07 KCNQ1 edels 91 3 chr11: 2422797-2826915 11p15.5 No 0.34 KCTD19 gdups 149 3 chr16: 65880894-65918162 16q22.1 No 0.07 KCTD5 edups 140 5 chr16: 2672499-2699030 16p13.3 No 0.01 KIAA0195 gdups 160 9 chr17: 70964317-71007758 17q25.1 No 3.30E−04 KIAA0319 edups 52 5 chr6: 24652311-24754362 6p22.2 No 0.01 KIAA0528 edels 113 2 chr12: 22492808-22588719 12p12.1 No 0.78 KIAA1086 gdups 173 3 chr19: 3755022-3820027 19p13.3 No 0.07 KIAA1586 edels 54 3 chr6: 57019343-57027951 6p12.1 No 0.01 KIAA1856 edups 61 4 chr7: 5312949-5429703 7p22.1 No 0.10 KLHL22 gdups 203 3 chr22: 19125806-19180122 22q11.21 Yes 0.02 KREMEN2 edels 141 3 chr16: 2954218-2958381 16p13.3 No 1.96E−03 KRTAP13-2 gdups 199 2 chr21: 30665580-30666446 21q22.11 Yes 0.17 KRTAP23-1 gdups 199 2 chr21: 30642598-30642795 21q22.11 Yes 0.17 KRTAP24-1 gdups 199 2 chr21: 30575498-30577147 21q22.11 Yes 0.17 KRTAP26-1 gdups 199 2 chr21: 30613313-30614505 21q22.11 Yes 0.17 KRTAP27-1 gdups 199 2 chr21: 30631202-30631883 21q22.11 Yes 0.17 KRTHB1 gdups 114 3 chr12: 50965964-50971566 12q13.13 No 0.19 LAMA2 edels 57 2 chr6: 129245979-129879401 6q22.33 Yes 0.17 LFNG gdups 59 6 chr7: 2518689-2535334 7p22.2 No 4.79E−03 LILRA3 gdups 192 4 chr19: 59491666-59501764 19q13.42 No 0.64 LILRA5 gdups 192 4 chr19: 59510165-59516221 19q13.42 No 0.64 LMTK3 gdups 190 4 chr19: 53680340-53708258 19q13.32 No 0.03 LOC128977 gdups 203 3 chr22: 17808417-17815220 22q11.21 Yes 1.96E−03 LOC150383 gdups 207 3 chr22: 45018574-45024857 22q13.31 No 0.07 LOC162073 edels 145 3 chr16: 19032783-19040453 16p12.3 No 0.07 LOC283849 gdups 148 12 chr16: 65767006-65775384 16q22.1 No 2.27E−05 LOC285498 gdups 39 3 chr4: 1056544-1097350 4p16.3 Yes 0.03 LOC388910 gdups 205 2 chr22: 43343883-43346993 22q13.31 No 0.17 LOC389852 gdups 211 3 chrX: 47871547-47876941 Xp11.23 Yes 0.07 LOC650137 edels 129 26 chr15: 19915066-19915749 15q11.2 Yes 3.31E−11 LOC653319 gdups 148 10 chr16: 65775770-65781608 16q22.1 No 1.35E−04 LOC728489 gdups 81 5 chr9: 138376173-138378062 9q34.3 Yes 4.79E−03 LOC728912 gdups 15 3 chr1: 146040948-146076705 1q21.1 Yes 0.01 LOC728932 gdups 15 3 chr1: 145907791-145932379 1q21.1 Yes 0.01 LOC93343 gdups 179 5 chr19: 17393714-17397140 19p13.11 No 0.01 LRBA edels 43 2 chr4: 151405044-152156329 4q31.3 No 0.68 LRP3 gdups 184 3 chr19: 38377330-38390383 19q13.11 Yes 0.07 LRP5 edups 104 3 chr11: 67836684-67973315 11q13.2 No 0.07 LRRC27 edups 89 2 chr10: 133995648-134109058 10q26.3 No 0.17 LRRC29 gdups 148 12 chr16: 65798543-65818414 16q22.1 No 2.27E−05 LRRC36 gdups 149 3 chr16: 65918248-65976604 16q22.1 No 0.07 LRTM2 gdups 109 3 chr12: 1799956-1816179 12p13.33 Yes 0.07 LYG1 gdups 27 3 chr2: 99267134-99287637 2q11.2 Yes 0.19 LYG2 gdups 27 3 chr2: 99225141-99238034 2q11.2 Yes 0.19 MADCAM1 edels 167 3 chr19: 447490-456340 19p13.3 No 5.54E−05 MAGEA11 gdups 212 2 chrX: 148575479-148603920 Xq28 Yes 0.17 MAGEL2 gdups 131 5 chr15: 21439789-21442268 15q11.2 Yes 9.28E−06 MAP2K2 gdups 173 7 chr19: 4041319-4075126 19p13.3 No 1.96E−03 MAPK8IP1 gdups 96 5 chr11: 45863778-45884592 11p11.2 No 0.01 MAST4 edels 47 2 chr5: 65927932-66501179 5q12.3 No 0.17 MATK gdups 173 3 chr19: 3728968-3752810 19p13.3 No 0.07 MDGA2 edels 128 8 chr14: 46379045-47213703 14q21.3 No 1.35E−04 METAP2 edups 117 2 chr12: 94391953-94433746 12q22 No 0.17 MGC10992 edups 147 3 chr16: 56103591-56127978 16q13 No 0.07 MGC11335 gdups 150 3 chr16: 66265940-66310720 16q22.1 No 0.07 MGMT edups 88 4 chr10: 131155510-131455356 10q26.3 Yes 0.03 MIOX gdups 208 4 chr22: 49272079-49275943 22q13.33 Yes 0.03 MKRN3 gdups 131 5 chr15: 21361547-21364653 15q11.2 Yes 9.28E−06 MOCOS edups 166 3 chr18: 32021478-32102682 18q12.2 No 0.07 MPDZ edels 75 2 chr9: 13095703-13269563 9p23 Yes 0.37 MRPL40 gdups 203 3 chr22: 17800036-17803594 22q11.21 Yes 1.96E−03 MRPL54 gdups 173 3 chr19: 3713665-3718562 19p13.3 No 0.07 MSMB gdups 84 2 chr10: 51219559-51232596 10q11.23 Yes 0.17 MUM1 gdups 169 4 chr19: 1300175-1329427 19p13.3 Yes 0.03 MYLK2 gdups 193 2 chr20: 29870772-29886153 20q11.21 No 0.17 NBPF11 gdups 15 3 chr1: 146040948-146076705 1q21.1 Yes 0.01 NCOA4 gdups 84 2 chr10: 51235233-51260740 10q11.23 Yes 0.17 NDN gdups 131 5 chr15: 21481916-21483570 15q11.2 Yes 2.27E−05 NDUFS7 gdups 169 4 chr19: 1334906-1346583 19p13.3 Yes 0.03 NEK3 edups 124 2 chr13: 51604780-51631997 13q14.3 No 0.17 NFIC edups 172 3 chr19: 3310616-3414603 19p13.3 Yes 0.07 NRXN1 edels 24 5 chr2: 50000992-51113178 2p16.3 Yes 3.30E−04 NUP210 edups 35 2 chr3: 13332737-13436809 3p25.1 No 0.17 NUTF2 gdups 150 3 chr16: 66438331-66462727 16q22.1 No 0.07 OBSCN edels 19 2 chr1: 226462484-226633198 1q42.13 No 0.54 OCA2 gdups 132 5 chr15: 25673622-26018053 15q13.1 Yes 2.27E−05 OPRD1 edups 10 5 chr1: 29011241-29062795 1p35.3 No 0.01 OR1C1 edels 21 3 chr1: 245987387-245988331 1q44 No 0.03 OR2AG1 edels 94 3 chr11: 6762845-6763795 11p15.4 No 0.07 OR2AG2 edels 94 3 chr11: 6745814-6746764 11p15.4 No 0.07 OR4C6 gdups 97 4 chr11: 55186202-55190738 11q11 No 0.54 OR4M2 edels 129 26 chr15: 19869940-19870881 15q11.2 Yes 3.31E−11 OR4N4 edels 129 26 chr15: 19804548-19885172 15q11.2 Yes 1.35E−11 OR4S2 gdups 97 9 chr11: 55174956-55175891 11q11 No 0.07 OSBPL5 edups 93 4 chr11: 3064922-3143116 11p15.4 No 0.03 PAMCI edels 116 2 chr12: 84722462-84754449 12q21.31 No 0.17 PAQR4 edels 141 3 chr16: 2959343-2963484 16p13.3 No 1.96E−03 PCDH9 edels 125 2 chr13: 65774970-66702578 13q21.32 Yes 0.17 PCQAP gdups 203 3 chr22: 19191886-19248975 22q11.21 Yes 4.79E−03 PI4KA gdups 203 3 chr22: 19391981-19543070 22q11.21 Yes 1.96E−03 PIK3R2 gdups 180 5 chr19: 18125016-18142343 19p13.11 No 0.01 PIM3 gdups 208 3 chr22: 48740165-48743721 22q13.33 Yes 0.07 PIP5K1C gdups 173 7 chr19: 3581182-3651445 19p13.3 No 1.96E−03 PKMYT1 edels 141 3 chr16: 2962793-2970506 16p13.3 No 1.96E−03 PLA2G4C edups 189 2 chr19: 53242916-53305865 19q13.32 No 0.17 PLEKHG4 gdups 148 12 chr16: 65868914-65880883 16q22.1 No 2.27E−05 PLEKHG5 edups 4 4 chr1: 6448739-6502708 1p36.31 No 0.03 PLEKHM2 edels 8 3 chr1: 15883414-15933849 1p36.21 No 0.34 POSTN edels 122 3 chr13: 37034779-37070874 13q13.3 No 0.07 PP2447 edups 208 5 chr22: 48966487-48980154 22q13.33 Yes 0.01 PP2447 gdups 208 8 chr22: 48966487-48980154 22q13.33 Yes 8.05E−04 PPME1 edups 105 4 chr11: 73619081-73643395 11q13.4 No 0.03 PRB3 edels 110 3 chr12: 11311393-11313908 12p13.2 No 0.07 PRDM10 edups 107 3 chr11: 129274817-129377940 11q24.3 No 0.07 PRIC285 edups 195 3 chr20: 61659883-61676036 20q13.33 Yes 0.03 PRKAB2 gdups 15 2 chr1: 145093314-145110753 1q21.1 Yes 0.01 PRKG1 edels 85 2 chr10: 52421124-53728116 10q11.23 Yes 0.17 PROP1 gdups 51 3 chr5: 177351842-177355849 5q35.3 No 0.07 PRR5 edups 206 3 chr22: 43443257-43637329 22q13.31 No 0.07 PSCD2 gdups 190 4 chr19: 53664424-53674457 19q13.32 No 0.03 PSKH1 gdups 150 4 chr16: 66484705-66521078 16q22.1 No 0.03 PSMD8 gdups 186 2 chr19: 43557016-43566304 19q13.2 No 0.17 QSOX2 edups 80 2 chr9: 138238006-138277508 9q34.3 Yes 0.07 RAB35 edups 118 3 chr12: 119017289-119038982 12q24.23 Yes 0.07 RAB39 gdups 106 2 chr11: 107304487-107339416 11q22.3 No 0.37 RABGAP1L edels 16 2 chr1: 172395171-173226353 1q25.1 No 0.99 RAI1 edups 156 5 chr17: 17525512-17655492 17p11.2 Yes 0.01 RANBP1 gdups 203 3 chr22: 18484947-18494878 22q11.21 Yes 1.96E−03 RANBP10 gdups 150 3 chr16: 66314506-66398056 16q22.1 No 0.07 RAX2 gdups 173 3 chr19: 3448813-3723219 19p13.3 No 0.07 RCD-8 gdups 150 4 chr16: 66464500-66475907 16q22.1 No 0.03 RNF111 edups 136 3 chr15: 57067157-57176541 15q22.1 Yes 0.07 RNF133 edels 68 3 chr7: 122125078-122126208 7q31.32 Yes 0.03 RNF148 edels 68 3 chr7: 122128956-122130257 7q31.32 Yes 0.03 RNF44 edups 50 5 chr5: 175886306-175897027 5q35.2 No 0.05 RPS15 gdups 169 8 chr19: 1389363-1391492 19p13.3 Yes 8.05E−04 RPS19 edups 187 3 chr19: 47055828-47067322 19q13.2 No 0.07 RYR2 edups 20 3 chr1: 235272128-236063911 1q43 No 0.34 SBF1 gdups 208 4 chr22: 49232050-49260330 22q13.33 Yes 0.03 SETD4 gdups 202 2 chr21: 36328709-36373557 21q22.12 Yes 0.17 SH3TC1 edups 41 2 chr4: 8251960-8293725 4p16.1 No 0.07 SIRT4 edups 119 2 chr12: 119224546-119235430 12q24.31 Yes 0.17 SKIV2L2 edels 46 6 chr5: 54639594-54757163 5q11.2 No 0.02 SLC16A5 edups 159 3 chr17: 70595650-70613841 17q25.1 No 0.07 SLC18A1 edels 70 2 chr8: 20046652-20084997 8p21.3 No 0.17 SLC22A18 edups 92 3 chr11: 2877527-2903052 11p15.4 No 0.03 SLC25A1 gdups 203 3 chr22: 17543092-17546260 22q11.21 Yes 1.96E−03 SLC25A34 edels 8 3 chr1: 15935396-15940471 1p36.21 No 0.34 SLC26A11 gdups 164 3 chr17: 75808824-75841890 17q25.3 No 0.07 SLC28A1 edups 137 2 chr15: 83228913-83290033 15q25.3 Yes 0.17 SLC2A4RG gdups 196 3 chr20: 61841655-61845846 20q13.33 Yes 0.07 SLC45A1 edups 5 2 chr1: 8300756-8326814 1p36.23 No 0.17 SLC6A15 edels 115 3 chr12: 83777402-83830705 12q21.31 No 0.19 SLC7A10 gdups 184 3 chr19: 38391410-38408596 19q13.11 Yes 0.07 SLC9A5 gdups 148 12 chr16: 65840356-65863594 16q22.1 No 2.27E−05 SLCO1A2 edels 112 3 chr12: 21311651-21439638 12p12.1 No 0.98 SLCO1B3 edups 111 2 chr12: 20854905-20960925 12p12.2 No 0.17 SMARCA4 edups 176 2 chr19: 10932606-11033953 19p13.2 No 0.17 SNRPN gdups 132 5 chr15: 22619887-22776293 15q11.2 Yes 9.28E−06 SNURF gdups 132 5 chr15: 22652824-22770696 15q11.2 Yes 9.28E−06 SNX25 edups 44 2 chr4: 186368278-186527942 4q35.1 Yes 0.17 SPACA5B gdups 211 3 chrX: 47875014-47876939 Xp11.23 Yes 0.07 SPON2 edels 40 5 chr4: 1150725-1156602 4p16.3 Yes 0.11 SPRED3 gdups 186 4 chr19: 43572779-43578711 19q13.2 No 0.03 SPRN gdups 90 2 chr10: 135084160-135088111 10q26.3 Yes 0.37 SRL edups 142 3 chr16: 4179378-4232077 16p13.3 No 0.07 SSSCA1 edels 101 3 chr11: 65094519-65095793 11q13.1 No 0.03 SSX5 gdups 211 3 chrX: 47930600-47941143 Xp11.23 Yes 0.07 STEAP3 edups 29 2 chr2: 119697854-119739698 2q14.2 No 0.37 STIP1 gdups 100 5 chr11: 63709873-63728596 11q13.1 No 0.01 SUCLG2 edels 37 2 chr3: 67507835-67787728 3p14.1 Yes 0.07 SYNGR2 gdups 162 3 chr17: 73676266-73680604 17q25.3 No 0.07 TCP10L gdups 200 3 chr21: 32870733-32879714 21q22.11 No 0.07 THAP11 gdups 150 3 chr16: 66433714-66435598 16q22.1 No 0.07 TJP3 gdups 173 5 chr19: 3672735-3701807 19p13.3 No 0.01 TMEM112 gdups 138 3 chr16: 843635-960985 16p13.3 Yes 0.07 TMEM138 gdups 98 2 chr11: 60886432-60893254 11q12.2 No 0.17 TNFRSF14 gdups 1 4 chr1: 2479153-2486757 1p36.32 Yes 0.03 TNFRSF8 edups 7 3 chr1: 12046021-12126851 1p36.22 No 0.07 TPPP edels 45 8 chr5: 712978-746510 5p15.33 Yes 4.61E−03 TRPM1 gdups 133 2 chr15: 29080845-29181216 15q13.3 Yes 0.37 TRPT1 gdups 100 5 chr11: 63747848-3750257 11q13.1 No 0.01 TSC2 edups 139 2 chr16: 2037991-2078713 16p13.3 No 0.17 TSNAXIP1 gdups 150 3 chr16: 66398511-66419471 16q22.1 No 0.07 TSSK2 gdups 203 3 chr22: 17498790-17500134 22q11.21 Yes 1.96E−03 TXNRD2 gdups 203 3 chr22: 18243040-18309359 22q11.21 Yes 1.96E−03 UBE2O edups 161 4 chr17: 71897491-71960883 17q25.1 No 0.03 UBE3A gdups 132 5 chr15: 23133489-23235221 15q11.2 Yes 9.28E−06 UBR1 edups 135 2 chr15: 41022398-41185578 15q15.2 No 0.37 UFD1L gdups 203 3 chr22: 17817701-17846726 22q11.21 Yes 1.96E−03 UGT1A5 edels 33 2 chr2: 234191093-234346688 2q37.1 No 0.17 UNC93B1 edels 103 3 chr11: 67515151-67528169 11q13.2 No 0.03 UNCX4.1 gdups 63 3 chr7: 1239180-1242734 7p22.3 Yes 0.07 UNQ2446 gdups 150 4 chr16: 66476282-66477772 16q22.1 No 0.03 URP2 gdups 100 5 chr11: 63730782-63747939 11q13.1 No 0.01 USH2A edels 17 3 chr1: 213862859-214663361 1q41 Yes 0.07 UTRN edups 58 2 chr6: 144654566-145215859 6q24.2 Yes 0.17 VCX2 gdups 210 3 chrX: 8097985-8099308 Xp22.31 No 0.07 VPS37B gdups 120 4 chr12: 121915835-121946665 12q24.31 Yes 0.03 WASF3 edups 121 5 chr13: 26029840-26161080 13q12.13 No 0.05 WDR78 edups 14 3 chr1: 67051162-67163158 1p31.3 No 0.07 WNT7A edups 36 3 chr3: 13835085-13896619 3p25.1 No 0.07 XG edels 209 2 chrX: 2680115-2743955 Xp22.33 Yes 0.17 ZC3H7B edups 204 5 chr22: 40027475-40086053 22q13.2 Yes 0.01 ZDHHC1 gdups 149 3 chr16: 65985829-66007878 16q22.1 No 0.07 ZNF208 gdups 182 2 chr19: 21940737-21985561 19p12 Yes 0.54 ZNF257 edels 183 2 chr19: 22027106-22064084 19p12 Yes 0.37 ZNF37A gdups 82 2 chr10: 38423281-38452282 10p11.21 No 0.17 ZNF676 edels 183 2 chr19: 22153743-22171593 19p12 Yes 0.17 ZNF74 gdups 203 3 chr22: 19078418-19092752 22q11.21 Yes 0.02

While certain preferred embodiments of the present invention have been described and specifically exemplified above, it is not intended that the invention be limited to such embodiments. Various modifications may be made to the invention without departing from the scope and spirit thereof as set forth in the following claims. 

1. A method for detecting a propensity for developing a neurological disorder, the method comprising: detecting the presence of at least one CNV in a target polynucleotide wherein if said CNV is present, said patient has an increased risk for developing a neurological disorder, wherein said deletion containing CNV is selected from the group of CNVs consisting of CNVs set forth in Table
 6. 2. The method as claimed in claim 1, wherein said at least one CNV is an edel selected from the group consisting of BZRAP1 Benzodiazapine receptor (peripheral) associated protein 1 17q22-q23 chr17:53733592-53761151, MDGA2 MAM domain containing glycosylphosphatidylinositol anchor 214q21.3 chr14:46,170,380-47,422,368, CLCNKA chloride channel Ka chr1:16221072-16233132, NTRK1 Neurotrophic tyrosine kinase, receptor, type 1 1q21-q22 chr1:155,013,407-155,202,154, USH2A Usher syndrome 2A (autosomal recessive, mild) 1q41 chr1:213,752,880-214,875,391, NRXN1 Neurexin 1 2p16.3 chr2:49,712,184-51,360,413, GALNT13 UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgal 2q23.3-q24.1 chr2:153,854,689-155,600,757, GMPS Guanine monophosphate synthetase 3q24 chr3:157,059,820-157,149,414, SPON2 Spondin 2, extracellular matrix protein 4p16.3 chr4:1,124,285-1,183,034, LRBA LPS-responsive vesicle trafficking, beach and anchor containin4q31.3 chr4:151,217,225-152,344,150, TPPP Tubulin polymerization promoting protein 5p15.3 chr5:567,501-892,810, SKIV2L2 Superkiller viralicidic activity 2-like 2 (S. cerevisiae) 5q11.2 chr5:54,522,183-54,873,752, KIAA1586 KIAA1586 6p12.1 chr6:56,980,593-57,066,702, BTN2A1 Butyrophilin, subfamily 2, member A1 6p22.1 chr6:26566167-26577844, BXDC1 Brix domain containing 1 6q21 chr6:111409983-111453487, LAMA2 Laminin, alpha 2 (merosin, congenital muscular dystrophy) 6q22-q23 chr6:128,945,101-130,370,307, DGKB Diacylglycerol kinase, beta 90 kDa 7p21.2 chr7:14,015,810-15,013,734, RNF133 Ring finger protein 133 7q31.32 chr7:122,118,508-122,132,937, RNF148 Ring finger protein 148 7₈31.33 chr7:122,118,508-122,132,937, SLC18A1 Solute carrier family 18 (vesicular monoamine), member 1 8p21.3 chr8:19,874,095-20,257,554, COL27A1 Collagen, type XXVII, alpha 1 9q32 chr9:115958051-116112796, OR2AG1 Olfactory receptor, family 2, subfamily AG, member 1 11p15.4 chr11:6762845-6763795, OR2AG2 Olfactory receptor, family 2, subfamily AG, member 2 11p15.4 chr11:6745814-6746764, SSSCA1 Sjogren syndrome/scleroderma autoantigen 1 11q13.1 chr11:65094518-65095815, FAM89B Family with sequence similarity 89, member B 11q23 chr11:65,094,554-65,100,079, PRB3 Proline-rich protein BstNI subfamily 3 12p13.2 chr12:11310124-11313908, KRT3 Keratin 3 12q12-q13 chr12:51,444,040-51,501,855, SLC6A15 Solute carrier family 6, member 15 12q21.3 chr12:83,670,976-83,958,489, DACH1 Dachshund homolog 1 (Drosophila) 13q22 chr13:70910098-71339331, LOC650137 Seven transmembrane helix receptor 15q11.2 chr15:19,812,808-20,018,007, OR4M2 Olfactory receptor, family 4, subfamily M, member 2 15q11.2 chr15:19,812,808-20,018,007, OR4N4 Hypothetical LOC727924 15q11.2 chr15:19,812,808-20,018,007, LOC162073 hypothetical protein LOC162073 16p12.3 chr16:19,008,005-19,060,144, DLGAP1 Discs, large (Drosophila) homolog-associated protein 1 18p11.3 chr18:3,393,512-3,965,460, FLJ44894 Homo sapiens cDNA FLJ44894 fis, clone BRAMY3000692, m 19p12 chr19:20,227,461-20,491,547, CYP4F22 Cytochrome P450, family 4, subfamily F, polypeptide 22 19p13.12 chr19:15480335-15524128, GRIK5 Glutamate receptor, ionotropic, kainate 5 19q13.2 chr19:47,126,828-47,329,282, GYG2 Glycogenin 2 Xp22.3 chrX:2,656,547-2,925,352, XG Xg pseudogene, Y-linked 2 Xp22.33 chrX:2,656,547-2,925,353, FGF13 Fibroblast growth factor 13 Xq26.3 chrX:137,421,326-138,459,367, SPANXB1 SPANX family, member B2 Xq27.1 chrX:139,908,245-139,941,724, and SPANXB2 SPANX family, member B2 Xq27.1 chrX:139,908,245-139,941,724.
 3. The method of claim 1, wherein said neurological disorder is selected from the group consisting of autism, autism spectrum disorder (ASD), schizophrenia, bipolar disorder, Tourette Syndrome, and obsessive compulsive disorder.
 4. The method of claim 2, wherein said disorder is autism spectrum disorder.
 5. The method as claimed in claim 1, wherein the target nucleic acid is amplified prior to detection.
 6. The method of claim 1, wherein the step of detecting the presence of said CNV is performed using a process selected from the group consisting of detection of specific hybridization, measurement of allele size, restriction fragment length polymorphism analysis, allele-specific hybridization analysis, single base primer extension reaction, and sequencing of an amplified polynucleotide.
 7. The method as claimed in claim 1 or 2, wherein in the target nucleic acid is DNA.
 8. The method of claim 1, wherein nucleic acids comprising said CNV are obtained from an isolated cell of the human subject.
 9. A method for identifying therapeutic agents which alter neuronal signaling and/or morphology, comprising a) providing cells expressing at least one CNV as claimed in claim 1; b) providing cells which express the cognate wild type sequences corresponding to the CNV of step a); c) contacting the cells of steps a) and b) with a test agent and d) analyzing whether said agent alters neuronal signaling and/or morphology of cells of step a) relative to those of step b), thereby identifying agents which alter neuronal signaling and morphology.
 10. The method of claim 9 wherein said agent has efficacy for the treatment of neurodevelopmental disorders.
 11. A test agent identified by claim 9 in a pharmaceutically acceptable carrier.
 12. A method for the treatment of a neurological disorder in a patient in need thereof comprising administration of an effective amount of the agent of claim
 11. 13. The method of claim 9, wherein said agent modulates neuronal cell signaling.
 14. A vector comprising at least one of the CNV-containing nucleic acids of claim
 1. 15. A host cell comprising the vector of claim
 14. 16. A solid support comprising the neurological disorder related CNV containing nucleic acid of claim
 1. 17. The method of claim 9, wherein said CNV is an edel in BZRAP1 or MDGA2.
 18. The method of claim 9, wherein said CNV is an edel in NRXN1.
 19. The method of claim 9, wherein said CNV is an edel in GRIK5. 